Canonical Allele Identifier: CA351204538

Gene: LRRFIP1

Linked Data

• MyVariant Identifiers: chr2:g.238672530G>T (hg19) ; chr2:g.237763887G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237763887G>T , CM000664.2:g.237763887G>T	GRCh38
NC_000002.11:g.238672530G>T , CM000664.1:g.238672530G>T	GRCh37
NC_000002.10:g.238337269G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698097.1:c.1181+3682G>T
ENST00000698098.1:c.955+3682G>T	ENSP00000513562.1:n.955+3682G>T
ENST00000308482.14:c.1459+3682G>T MANE Select	ENSP00000310109.9:n.1459+3682G>T
ENST00000244815.9:c.2102G>T	ENSP00000244815.5:p.Arg701Leu
ENST00000289175.10:c.2006G>T	ENSP00000289175.6:p.Arg669Leu
ENST00000308482.13:c.1459+3682G>T	ENSP00000310109.9:n.1459+3682G>T
ENST00000392000.4:c.2174G>T	ENSP00000375857.4:p.Arg725Leu
ENST00000483443.1:n.235+3682G>T
NM_001137550.1:c.1459+3682G>T	NP_001131022.1:n.1459+3682G>T
NM_001137551.1:c.721+3682G>T	NP_001131023.1:n.721+3682G>T
NM_001137552.1:c.2174G>T	NP_001131024.1:p.Arg725Leu
NM_001137553.1:c.2006G>T	NP_001131025.1:p.Arg669Leu
NM_004735.3:c.2102G>T	NP_004726.2:p.Arg701Leu
XM_005246112.3:c.2807G>T	XP_005246169.1:p.Arg936Leu
XM_005246115.3:c.2762G>T	XP_005246172.1:p.Arg921Leu
XM_005246116.3:c.2744G>T	XP_005246173.1:p.Arg915Leu
XM_005246118.3:c.2699G>T	XP_005246175.1:p.Arg900Leu
XM_005246119.3:c.2696G>T	XP_005246176.1:p.Arg899Leu
XM_005246120.3:c.2660G>T	XP_005246177.1:p.Arg887Leu
XM_005246121.3:c.2645G>T	XP_005246178.1:p.Arg882Leu
XM_005246122.3:c.2633G>T	XP_005246179.1:p.Arg878Leu
XM_005246124.1:c.2615G>T	XP_005246181.1:p.Arg872Leu
XM_005246125.3:c.2594G>T	XP_005246182.1:p.Arg865Leu
XM_005246126.3:c.2555G>T	XP_005246183.1:p.Arg852Leu
XM_005246128.1:c.2522G>T	XP_005246185.1:p.Arg841Leu
XM_005246129.3:c.2483G>T	XP_005246186.1:p.Arg828Leu
XM_005246130.3:c.2456G>T	XP_005246187.1:p.Arg819Leu
XM_005246131.3:c.2369G>T	XP_005246188.1:p.Arg790Leu
XM_005246132.3:c.2294G>T	XP_005246189.1:p.Arg765Leu
XM_005246133.1:c.2264G>T	XP_005246190.1:p.Arg755Leu
XM_005246134.1:c.2222G>T	XP_005246191.1:p.Arg741Leu
XM_005246135.1:c.2192G>T	XP_005246192.1:p.Arg731Leu
XM_005246136.1:c.2036G>T	XP_005246193.1:p.Arg679Leu
XM_005246141.3:c.823+3682G>T	XP_005246198.1:n.823+3682G>T
XM_005246142.1:c.751+3682G>T	XP_005246199.1:n.751+3682G>T
XM_006712842.2:c.2705G>T	XP_006712905.1:p.Arg902Leu
XM_006712843.2:c.2600G>T	XP_006712906.1:p.Arg867Leu
XM_006712844.1:c.2534G>T	XP_006712907.1:p.Arg845Leu
XM_006712845.2:c.2516G>T	XP_006712908.1:p.Arg839Leu
XM_006712846.1:c.2420G>T	XP_006712909.1:p.Arg807Leu
XM_006712847.1:c.2360G>T	XP_006712910.1:p.Arg787Leu
XM_006712848.1:c.2288G>T	XP_006712911.1:p.Arg763Leu
XM_011512152.1:c.2840G>T	XP_011510454.1:p.Arg947Leu
XM_011512153.1:c.2822G>T	XP_011510455.1:p.Arg941Leu
XM_011512154.1:c.2810G>T	XP_011510456.1:p.Arg937Leu
XM_011512155.1:c.2801G>T	XP_011510457.1:p.Arg934Leu
XM_011512156.1:c.2768G>T	XP_011510458.1:p.Arg923Leu
XM_011512157.1:c.2654G>T	XP_011510459.1:p.Arg885Leu
XM_011512158.1:c.2582G>T	XP_011510460.1:p.Arg861Leu
XM_011512159.1:c.2390G>T	XP_011510461.1:p.Arg797Leu
XM_011512160.1:c.1555+3682G>T	XP_011510462.1:n.1555+3682G>T
XM_011512161.1:c.1555+3682G>T	XP_011510463.1:n.1555+3682G>T
XM_011512162.1:c.1369+3682G>T	XP_011510464.1:n.1369+3682G>T
XM_011512163.1:c.1297+3682G>T	XP_011510465.1:n.1297+3682G>T
XM_011512164.1:c.751+3682G>T	XP_011510466.1:n.751+3682G>T
XM_011512165.1:c.721+3682G>T	XP_011510467.1:n.721+3682G>T
XM_011512166.1:c.1516+3682G>T	XP_011510468.1:n.1516+3682G>T
XR_923063.1:n.1605+3682G>T
XM_005246141.4:c.823+3682G>T	XP_005246198.1:n.823+3682G>T
XM_005246142.2:c.751+3682G>T	XP_005246199.1:n.751+3682G>T
XM_017005253.2:c.1522+3682G>T	XP_016860742.1:n.1522+3682G>T
XM_017005254.2:c.1522+3682G>T	XP_016860743.1:n.1522+3682G>T
XM_017005255.2:c.1450+3682G>T	XP_016860744.1:n.1450+3682G>T
XM_017005256.2:c.1336+3682G>T	XP_016860745.1:n.1336+3682G>T
XM_017005257.2:c.1387+3682G>T	XP_016860746.1:n.1387+3682G>T
XM_017005258.2:c.1336+3682G>T	XP_016860747.1:n.1336+3682G>T
XM_017005260.2:c.1162+3682G>T	XP_016860749.1:n.1162+3682G>T
XM_017005261.2:c.1099+3682G>T	XP_016860750.1:n.1099+3682G>T
XM_017005262.2:c.1099+3682G>T	XP_016860751.1:n.1099+3682G>T
XM_017005263.2:c.937+3682G>T	XP_016860752.1:n.937+3682G>T
XR_001739039.2:n.2876G>T
XR_001739040.1:n.3041G>T
XR_001739041.2:n.2837G>T
XR_001739042.2:n.2813G>T
XR_001739043.1:n.2789G>T
XR_001739044.2:n.2804G>T
XR_001739045.2:n.2774G>T
XR_001739046.1:n.3121G>T
XR_001739047.2:n.2690G>T
XR_001739048.1:n.2879G>T
XR_001739049.2:n.2624G>T
XR_001739050.2:n.2585G>T
XR_001739051.2:n.2552G>T
XR_001739052.2:n.2525G>T
XR_001739053.1:n.2514G>T
XR_001739054.1:n.2436G>T
XR_001739055.2:n.2453G>T
XR_001739056.2:n.2438G>T
XR_001739057.1:n.2454G>T
XR_001739058.1:n.2633G>T
XR_001739059.2:n.2366G>T
XR_001739060.1:n.2340G>T
XR_001739061.1:n.2382G>T
XR_001739062.1:n.2559G>T
XR_001739063.1:n.2266G>T
XR_001739064.1:n.2527G>T
XR_001739065.1:n.2471G>T
XR_001739066.1:n.2268G>T
XR_001739067.1:n.2175G>T
XR_001739068.1:n.2196G>T
XR_001739069.1:n.2373G>T
XR_001739070.1:n.2237G>T
XR_001739071.1:n.2095G>T
XR_001739072.1:n.2341G>T
XR_001739073.2:n.1591+3682G>T
XR_002959364.1:n.2267G>T
NM_001137550.2:c.1459+3682G>T MANE Select	NP_001131022.1:n.1459+3682G>T
NM_001137552.2:c.2174G>T	NP_001131024.1:p.Arg725Leu
NM_001137553.2:c.2006G>T	NP_001131025.1:p.Arg669Leu
NM_004735.4:c.2102G>T	NP_004726.2:p.Arg701Leu
NM_001137551.2:c.721+3682G>T	NP_001131023.1:n.721+3682G>T