Canonical Allele Identifier: CA385181567

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56086975C>T (hg19) ; chr12:g.55693191C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693191C>T , CM000674.2:g.55693191C>T	GRCh38
NC_000012.11:g.56086975C>T , CM000674.1:g.56086975C>T	GRCh37
NC_000012.10:g.54373242C>T	NCBI36
NG_012343.1:g.24115G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2286G>A	ENSP00000452467.1:n.*2286G>A
ENST00000554327.6:c.1333G>A
ENST00000557058.2:n.2077G>A
ENST00000557257.2:c.2188G>A	ENSP00000450578.2:p.Gly730Arg
ENST00000557555.3:c.2674G>A	ENSP00000451039.3:p.Gly892Arg
ENST00000686981.1:c.*2373G>A	ENSP00000510795.1:n.*2373G>A
ENST00000687390.1:n.768G>A
ENST00000691052.1:c.*1146G>A	ENSP00000508886.1:n.*1146G>A
ENST00000691846.1:c.1475G>A
ENST00000691973.1:c.2652+22G>A	ENSP00000509141.1:n.2652+22G>A
ENST00000257879.11:c.2662G>A MANE Select	ENSP00000257879.7:p.Gly888Arg
ENST00000553804.6:c.2674G>A	ENSP00000452120.1:p.Gly892Arg
ENST00000257879.10:c.2662G>A	ENSP00000257879.6:p.Gly888Arg
ENST00000347027.10:c.2644G>A	ENSP00000343009.6:p.Gly882Arg
ENST00000452168.6:c.2383G>A	ENSP00000393844.2:p.Gly795Arg
ENST00000553804.5:c.2674G>A	ENSP00000452120.1:p.Gly892Arg
ENST00000554327.5:c.727G>A
ENST00000555728.5:c.2794G>A	ENSP00000452387.1:p.Gly932Arg
NM_001144996.1:c.2674G>A	NP_001138468.1:p.Gly892Arg
NM_001144997.1:c.2383G>A	NP_001138469.1:p.Gly795Arg
NM_002206.2:c.2662G>A	NP_002197.2:p.Gly888Arg
XM_005268839.1:c.2794G>A	XP_005268896.1:p.Gly932Arg
XM_005268840.1:c.2776G>A	XP_005268897.1:p.Gly926Arg
XM_005268841.1:c.2794G>A	XP_005268898.1:p.Gly932Arg
XM_005268842.1:c.2644G>A	XP_005268899.1:p.Gly882Arg
XM_005268844.1:c.2455G>A	XP_005268901.1:p.Gly819Arg
XM_005268845.1:c.2323G>A	XP_005268902.1:p.Gly775Arg
XM_005268846.1:c.2323G>A	XP_005268903.1:p.Gly775Arg
XM_005268847.1:c.2320G>A	XP_005268904.1:p.Gly774Arg
XM_005268848.1:c.2320G>A	XP_005268905.1:p.Gly774Arg
XM_005268849.1:c.2320G>A	XP_005268906.1:p.Gly774Arg
XM_005268850.1:c.2188G>A	XP_005268907.1:p.Gly730Arg
XM_011538286.1:c.2455G>A	XP_011536588.1:p.Gly819Arg
XM_005268839.2:c.2794G>A	XP_005268896.1:p.Gly932Arg
XM_005268840.2:c.2776G>A	XP_005268897.1:p.Gly926Arg
XM_005268841.2:c.2794G>A	XP_005268898.1:p.Gly932Arg
XM_005268842.2:c.2644G>A	XP_005268899.1:p.Gly882Arg
XM_017019265.1:c.2404G>A	XP_016874754.1:p.Gly802Arg
NM_001144996.2:c.2674G>A	NP_001138468.1:p.Gly892Arg
NM_001367993.1:c.2335G>A	NP_001354922.1:p.Gly779Arg
NM_001367994.1:c.1318G>A	NP_001354923.1:p.Gly440Arg
NM_001374465.1:c.2644G>A	NP_001361394.1:p.Gly882Arg
NM_002206.3:c.2662G>A MANE Select	NP_002197.2:p.Gly888Arg