Canonical Allele Identifier: CA351204665
Gene: LRRFIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237763914C>G , CM000664.2:g.237763914C>G GRCh38
NC_000002.11:g.238672557C>G , CM000664.1:g.238672557C>G GRCh37
NC_000002.10:g.238337296C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000698097.1:c.1181+3709C>G
ENST00000698098.1:c.955+3709C>G ENSP00000513562.1:n.955+3709C>G
ENST00000308482.14:c.1459+3709C>G MANE Select ENSP00000310109.9:n.1459+3709C>G
ENST00000244815.9:c.2129C>G ENSP00000244815.5:p.Pro710Arg
ENST00000289175.10:c.2033C>G ENSP00000289175.6:p.Pro678Arg
ENST00000308482.13:c.1459+3709C>G ENSP00000310109.9:n.1459+3709C>G
ENST00000392000.4:c.2201C>G ENSP00000375857.4:p.Pro734Arg
ENST00000483443.1:n.235+3709C>G
NM_001137550.1:c.1459+3709C>G NP_001131022.1:n.1459+3709C>G
NM_001137551.1:c.721+3709C>G NP_001131023.1:n.721+3709C>G
NM_001137552.1:c.2201C>G NP_001131024.1:p.Pro734Arg
NM_001137553.1:c.2033C>G NP_001131025.1:p.Pro678Arg
NM_004735.3:c.2129C>G NP_004726.2:p.Pro710Arg
XM_005246112.3:c.2834C>G XP_005246169.1:p.Pro945Arg
XM_005246115.3:c.2789C>G XP_005246172.1:p.Pro930Arg
XM_005246116.3:c.2771C>G XP_005246173.1:p.Pro924Arg
XM_005246118.3:c.2726C>G XP_005246175.1:p.Pro909Arg
XM_005246119.3:c.2723C>G XP_005246176.1:p.Pro908Arg
XM_005246120.3:c.2687C>G XP_005246177.1:p.Pro896Arg
XM_005246121.3:c.2672C>G XP_005246178.1:p.Pro891Arg
XM_005246122.3:c.2660C>G XP_005246179.1:p.Pro887Arg
XM_005246124.1:c.2642C>G XP_005246181.1:p.Pro881Arg
XM_005246125.3:c.2621C>G XP_005246182.1:p.Pro874Arg
XM_005246126.3:c.2582C>G XP_005246183.1:p.Pro861Arg
XM_005246128.1:c.2549C>G XP_005246185.1:p.Pro850Arg
XM_005246129.3:c.2510C>G XP_005246186.1:p.Pro837Arg
XM_005246130.3:c.2483C>G XP_005246187.1:p.Pro828Arg
XM_005246131.3:c.2396C>G XP_005246188.1:p.Pro799Arg
XM_005246132.3:c.2321C>G XP_005246189.1:p.Pro774Arg
XM_005246133.1:c.2291C>G XP_005246190.1:p.Pro764Arg
XM_005246134.1:c.2249C>G XP_005246191.1:p.Pro750Arg
XM_005246135.1:c.2219C>G XP_005246192.1:p.Pro740Arg
XM_005246136.1:c.2063C>G XP_005246193.1:p.Pro688Arg
XM_005246141.3:c.823+3709C>G XP_005246198.1:n.823+3709C>G
XM_005246142.1:c.751+3709C>G XP_005246199.1:n.751+3709C>G
XM_006712842.2:c.2732C>G XP_006712905.1:p.Pro911Arg
XM_006712843.2:c.2627C>G XP_006712906.1:p.Pro876Arg
XM_006712844.1:c.2561C>G XP_006712907.1:p.Pro854Arg
XM_006712845.2:c.2543C>G XP_006712908.1:p.Pro848Arg
XM_006712846.1:c.2447C>G XP_006712909.1:p.Pro816Arg
XM_006712847.1:c.2387C>G XP_006712910.1:p.Pro796Arg
XM_006712848.1:c.2315C>G XP_006712911.1:p.Pro772Arg
XM_011512152.1:c.2867C>G XP_011510454.1:p.Pro956Arg
XM_011512153.1:c.2849C>G XP_011510455.1:p.Pro950Arg
XM_011512154.1:c.2837C>G XP_011510456.1:p.Pro946Arg
XM_011512155.1:c.2828C>G XP_011510457.1:p.Pro943Arg
XM_011512156.1:c.2795C>G XP_011510458.1:p.Pro932Arg
XM_011512157.1:c.2681C>G XP_011510459.1:p.Pro894Arg
XM_011512158.1:c.2609C>G XP_011510460.1:p.Pro870Arg
XM_011512159.1:c.2417C>G XP_011510461.1:p.Pro806Arg
XM_011512160.1:c.1555+3709C>G XP_011510462.1:n.1555+3709C>G
XM_011512161.1:c.1555+3709C>G XP_011510463.1:n.1555+3709C>G
XM_011512162.1:c.1369+3709C>G XP_011510464.1:n.1369+3709C>G
XM_011512163.1:c.1297+3709C>G XP_011510465.1:n.1297+3709C>G
XM_011512164.1:c.751+3709C>G XP_011510466.1:n.751+3709C>G
XM_011512165.1:c.721+3709C>G XP_011510467.1:n.721+3709C>G
XM_011512166.1:c.1516+3709C>G XP_011510468.1:n.1516+3709C>G
XR_923063.1:n.1605+3709C>G
XM_005246141.4:c.823+3709C>G XP_005246198.1:n.823+3709C>G
XM_005246142.2:c.751+3709C>G XP_005246199.1:n.751+3709C>G
XM_017005253.2:c.1522+3709C>G XP_016860742.1:n.1522+3709C>G
XM_017005254.2:c.1522+3709C>G XP_016860743.1:n.1522+3709C>G
XM_017005255.2:c.1450+3709C>G XP_016860744.1:n.1450+3709C>G
XM_017005256.2:c.1336+3709C>G XP_016860745.1:n.1336+3709C>G
XM_017005257.2:c.1387+3709C>G XP_016860746.1:n.1387+3709C>G
XM_017005258.2:c.1336+3709C>G XP_016860747.1:n.1336+3709C>G
XM_017005260.2:c.1162+3709C>G XP_016860749.1:n.1162+3709C>G
XM_017005261.2:c.1099+3709C>G XP_016860750.1:n.1099+3709C>G
XM_017005262.2:c.1099+3709C>G XP_016860751.1:n.1099+3709C>G
XM_017005263.2:c.937+3709C>G XP_016860752.1:n.937+3709C>G
XR_001739039.2:n.2903C>G
XR_001739040.1:n.3068C>G
XR_001739041.2:n.2864C>G
XR_001739042.2:n.2840C>G
XR_001739043.1:n.2816C>G
XR_001739044.2:n.2831C>G
XR_001739045.2:n.2801C>G
XR_001739046.1:n.3148C>G
XR_001739047.2:n.2717C>G
XR_001739048.1:n.2906C>G
XR_001739049.2:n.2651C>G
XR_001739050.2:n.2612C>G
XR_001739051.2:n.2579C>G
XR_001739052.2:n.2552C>G
XR_001739053.1:n.2541C>G
XR_001739054.1:n.2463C>G
XR_001739055.2:n.2480C>G
XR_001739056.2:n.2465C>G
XR_001739057.1:n.2481C>G
XR_001739058.1:n.2660C>G
XR_001739059.2:n.2393C>G
XR_001739060.1:n.2367C>G
XR_001739061.1:n.2409C>G
XR_001739062.1:n.2586C>G
XR_001739063.1:n.2293C>G
XR_001739064.1:n.2554C>G
XR_001739065.1:n.2498C>G
XR_001739066.1:n.2295C>G
XR_001739067.1:n.2202C>G
XR_001739068.1:n.2223C>G
XR_001739069.1:n.2400C>G
XR_001739070.1:n.2264C>G
XR_001739071.1:n.2122C>G
XR_001739072.1:n.2368C>G
XR_001739073.2:n.1591+3709C>G
XR_002959364.1:n.2294C>G
NM_001137550.2:c.1459+3709C>G MANE Select NP_001131022.1:n.1459+3709C>G
NM_001137552.2:c.2201C>G NP_001131024.1:p.Pro734Arg
NM_001137553.2:c.2033C>G NP_001131025.1:p.Pro678Arg
NM_004735.4:c.2129C>G NP_004726.2:p.Pro710Arg
NM_001137551.2:c.721+3709C>G NP_001131023.1:n.721+3709C>G