Canonical Allele Identifier: CA431937331

Gene: LRRFIP1

Linked Data

• MyVariant Identifiers: chr2:g.238672555T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237763912T>C , CM000664.2:g.237763912T>C	GRCh38
NC_000002.11:g.238672555T>C , CM000664.1:g.238672555T>C	GRCh37
NC_000002.10:g.238337294T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698097.1:c.1181+3707T>C
ENST00000698098.1:c.955+3707T>C	ENSP00000513562.1:n.955+3707T>C
ENST00000308482.14:c.1459+3707T>C MANE Select	ENSP00000310109.9:n.1459+3707T>C
ENST00000244815.9:c.2127T>C	ENSP00000244815.5:p.Ser709=
ENST00000289175.10:c.2031T>C	ENSP00000289175.6:p.Ser677=
ENST00000308482.13:c.1459+3707T>C	ENSP00000310109.9:n.1459+3707T>C
ENST00000392000.4:c.2199T>C	ENSP00000375857.4:p.Ser733=
ENST00000483443.1:n.235+3707T>C
NM_001137550.1:c.1459+3707T>C	NP_001131022.1:n.1459+3707T>C
NM_001137551.1:c.721+3707T>C	NP_001131023.1:n.721+3707T>C
NM_001137552.1:c.2199T>C	NP_001131024.1:p.Ser733=
NM_001137553.1:c.2031T>C	NP_001131025.1:p.Ser677=
NM_004735.3:c.2127T>C	NP_004726.2:p.Ser709=
XM_005246112.3:c.2832T>C	XP_005246169.1:p.Ser944=
XM_005246115.3:c.2787T>C	XP_005246172.1:p.Ser929=
XM_005246116.3:c.2769T>C	XP_005246173.1:p.Ser923=
XM_005246118.3:c.2724T>C	XP_005246175.1:p.Ser908=
XM_005246119.3:c.2721T>C	XP_005246176.1:p.Ser907=
XM_005246120.3:c.2685T>C	XP_005246177.1:p.Ser895=
XM_005246121.3:c.2670T>C	XP_005246178.1:p.Ser890=
XM_005246122.3:c.2658T>C	XP_005246179.1:p.Ser886=
XM_005246124.1:c.2640T>C	XP_005246181.1:p.Ser880=
XM_005246125.3:c.2619T>C	XP_005246182.1:p.Ser873=
XM_005246126.3:c.2580T>C	XP_005246183.1:p.Ser860=
XM_005246128.1:c.2547T>C	XP_005246185.1:p.Ser849=
XM_005246129.3:c.2508T>C	XP_005246186.1:p.Ser836=
XM_005246130.3:c.2481T>C	XP_005246187.1:p.Ser827=
XM_005246131.3:c.2394T>C	XP_005246188.1:p.Ser798=
XM_005246132.3:c.2319T>C	XP_005246189.1:p.Ser773=
XM_005246133.1:c.2289T>C	XP_005246190.1:p.Ser763=
XM_005246134.1:c.2247T>C	XP_005246191.1:p.Ser749=
XM_005246135.1:c.2217T>C	XP_005246192.1:p.Ser739=
XM_005246136.1:c.2061T>C	XP_005246193.1:p.Ser687=
XM_005246141.3:c.823+3707T>C	XP_005246198.1:n.823+3707T>C
XM_005246142.1:c.751+3707T>C	XP_005246199.1:n.751+3707T>C
XM_006712842.2:c.2730T>C	XP_006712905.1:p.Ser910=
XM_006712843.2:c.2625T>C	XP_006712906.1:p.Ser875=
XM_006712844.1:c.2559T>C	XP_006712907.1:p.Ser853=
XM_006712845.2:c.2541T>C	XP_006712908.1:p.Ser847=
XM_006712846.1:c.2445T>C	XP_006712909.1:p.Ser815=
XM_006712847.1:c.2385T>C	XP_006712910.1:p.Ser795=
XM_006712848.1:c.2313T>C	XP_006712911.1:p.Ser771=
XM_011512152.1:c.2865T>C	XP_011510454.1:p.Ser955=
XM_011512153.1:c.2847T>C	XP_011510455.1:p.Ser949=
XM_011512154.1:c.2835T>C	XP_011510456.1:p.Ser945=
XM_011512155.1:c.2826T>C	XP_011510457.1:p.Ser942=
XM_011512156.1:c.2793T>C	XP_011510458.1:p.Ser931=
XM_011512157.1:c.2679T>C	XP_011510459.1:p.Ser893=
XM_011512158.1:c.2607T>C	XP_011510460.1:p.Ser869=
XM_011512159.1:c.2415T>C	XP_011510461.1:p.Ser805=
XM_011512160.1:c.1555+3707T>C	XP_011510462.1:n.1555+3707T>C
XM_011512161.1:c.1555+3707T>C	XP_011510463.1:n.1555+3707T>C
XM_011512162.1:c.1369+3707T>C	XP_011510464.1:n.1369+3707T>C
XM_011512163.1:c.1297+3707T>C	XP_011510465.1:n.1297+3707T>C
XM_011512164.1:c.751+3707T>C	XP_011510466.1:n.751+3707T>C
XM_011512165.1:c.721+3707T>C	XP_011510467.1:n.721+3707T>C
XM_011512166.1:c.1516+3707T>C	XP_011510468.1:n.1516+3707T>C
XR_923063.1:n.1605+3707T>C
XM_005246141.4:c.823+3707T>C	XP_005246198.1:n.823+3707T>C
XM_005246142.2:c.751+3707T>C	XP_005246199.1:n.751+3707T>C
XM_017005253.2:c.1522+3707T>C	XP_016860742.1:n.1522+3707T>C
XM_017005254.2:c.1522+3707T>C	XP_016860743.1:n.1522+3707T>C
XM_017005255.2:c.1450+3707T>C	XP_016860744.1:n.1450+3707T>C
XM_017005256.2:c.1336+3707T>C	XP_016860745.1:n.1336+3707T>C
XM_017005257.2:c.1387+3707T>C	XP_016860746.1:n.1387+3707T>C
XM_017005258.2:c.1336+3707T>C	XP_016860747.1:n.1336+3707T>C
XM_017005260.2:c.1162+3707T>C	XP_016860749.1:n.1162+3707T>C
XM_017005261.2:c.1099+3707T>C	XP_016860750.1:n.1099+3707T>C
XM_017005262.2:c.1099+3707T>C	XP_016860751.1:n.1099+3707T>C
XM_017005263.2:c.937+3707T>C	XP_016860752.1:n.937+3707T>C
XR_001739039.2:n.2901T>C
XR_001739040.1:n.3066T>C
XR_001739041.2:n.2862T>C
XR_001739042.2:n.2838T>C
XR_001739043.1:n.2814T>C
XR_001739044.2:n.2829T>C
XR_001739045.2:n.2799T>C
XR_001739046.1:n.3146T>C
XR_001739047.2:n.2715T>C
XR_001739048.1:n.2904T>C
XR_001739049.2:n.2649T>C
XR_001739050.2:n.2610T>C
XR_001739051.2:n.2577T>C
XR_001739052.2:n.2550T>C
XR_001739053.1:n.2539T>C
XR_001739054.1:n.2461T>C
XR_001739055.2:n.2478T>C
XR_001739056.2:n.2463T>C
XR_001739057.1:n.2479T>C
XR_001739058.1:n.2658T>C
XR_001739059.2:n.2391T>C
XR_001739060.1:n.2365T>C
XR_001739061.1:n.2407T>C
XR_001739062.1:n.2584T>C
XR_001739063.1:n.2291T>C
XR_001739064.1:n.2552T>C
XR_001739065.1:n.2496T>C
XR_001739066.1:n.2293T>C
XR_001739067.1:n.2200T>C
XR_001739068.1:n.2221T>C
XR_001739069.1:n.2398T>C
XR_001739070.1:n.2262T>C
XR_001739071.1:n.2120T>C
XR_001739072.1:n.2366T>C
XR_001739073.2:n.1591+3707T>C
XR_002959364.1:n.2292T>C
NM_001137550.2:c.1459+3707T>C MANE Select	NP_001131022.1:n.1459+3707T>C
NM_001137552.2:c.2199T>C	NP_001131024.1:p.Ser733=
NM_001137553.2:c.2031T>C	NP_001131025.1:p.Ser677=
NM_004735.4:c.2127T>C	NP_004726.2:p.Ser709=
NM_001137551.2:c.721+3707T>C	NP_001131023.1:n.721+3707T>C