Canonical Allele Identifier: CA385181564

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56086974C>A (hg19) ; chr12:g.55693190C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55693190C>A , CM000674.2:g.55693190C>A	GRCh38
NC_000012.11:g.56086974C>A , CM000674.1:g.56086974C>A	GRCh37
NC_000012.10:g.54373241C>A	NCBI36
NG_012343.1:g.24116G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*2287G>T	ENSP00000452467.1:n.*2287G>T
ENST00000554327.6:c.1334G>T
ENST00000557058.2:n.2078G>T
ENST00000557257.2:c.2189G>T	ENSP00000450578.2:p.Gly730Val
ENST00000557555.3:c.2675G>T	ENSP00000451039.3:p.Gly892Val
ENST00000686981.1:c.*2374G>T	ENSP00000510795.1:n.*2374G>T
ENST00000687390.1:n.769G>T
ENST00000691052.1:c.*1147G>T	ENSP00000508886.1:n.*1147G>T
ENST00000691846.1:c.1476G>T
ENST00000691973.1:c.2652+23G>T	ENSP00000509141.1:n.2652+23G>T
ENST00000257879.11:c.2663G>T MANE Select	ENSP00000257879.7:p.Gly888Val
ENST00000553804.6:c.2675G>T	ENSP00000452120.1:p.Gly892Val
ENST00000257879.10:c.2663G>T	ENSP00000257879.6:p.Gly888Val
ENST00000347027.10:c.2645G>T	ENSP00000343009.6:p.Gly882Val
ENST00000452168.6:c.2384G>T	ENSP00000393844.2:p.Gly795Val
ENST00000553804.5:c.2675G>T	ENSP00000452120.1:p.Gly892Val
ENST00000554327.5:c.728G>T
ENST00000555728.5:c.2795G>T	ENSP00000452387.1:p.Gly932Val
NM_001144996.1:c.2675G>T	NP_001138468.1:p.Gly892Val
NM_001144997.1:c.2384G>T	NP_001138469.1:p.Gly795Val
NM_002206.2:c.2663G>T	NP_002197.2:p.Gly888Val
XM_005268839.1:c.2795G>T	XP_005268896.1:p.Gly932Val
XM_005268840.1:c.2777G>T	XP_005268897.1:p.Gly926Val
XM_005268841.1:c.2795G>T	XP_005268898.1:p.Gly932Val
XM_005268842.1:c.2645G>T	XP_005268899.1:p.Gly882Val
XM_005268844.1:c.2456G>T	XP_005268901.1:p.Gly819Val
XM_005268845.1:c.2324G>T	XP_005268902.1:p.Gly775Val
XM_005268846.1:c.2324G>T	XP_005268903.1:p.Gly775Val
XM_005268847.1:c.2321G>T	XP_005268904.1:p.Gly774Val
XM_005268848.1:c.2321G>T	XP_005268905.1:p.Gly774Val
XM_005268849.1:c.2321G>T	XP_005268906.1:p.Gly774Val
XM_005268850.1:c.2189G>T	XP_005268907.1:p.Gly730Val
XM_011538286.1:c.2456G>T	XP_011536588.1:p.Gly819Val
XM_005268839.2:c.2795G>T	XP_005268896.1:p.Gly932Val
XM_005268840.2:c.2777G>T	XP_005268897.1:p.Gly926Val
XM_005268841.2:c.2795G>T	XP_005268898.1:p.Gly932Val
XM_005268842.2:c.2645G>T	XP_005268899.1:p.Gly882Val
XM_017019265.1:c.2405G>T	XP_016874754.1:p.Gly802Val
NM_001144996.2:c.2675G>T	NP_001138468.1:p.Gly892Val
NM_001367993.1:c.2336G>T	NP_001354922.1:p.Gly779Val
NM_001367994.1:c.1319G>T	NP_001354923.1:p.Gly440Val
NM_001374465.1:c.2645G>T	NP_001361394.1:p.Gly882Val
NM_002206.3:c.2663G>T MANE Select	NP_002197.2:p.Gly888Val