Canonical Allele Identifier: CA385188535

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56090828T>C (hg19) ; chr12:g.55697044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55697044T>C , CM000674.2:g.55697044T>C	GRCh38
NC_000012.11:g.56090828T>C , CM000674.1:g.56090828T>C	GRCh37
NC_000012.10:g.54377095T>C	NCBI36
NG_012343.1:g.20262A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.*1216A>G	ENSP00000452467.1:n.*1216A>G
ENST00000554327.6:c.456A>G
ENST00000557058.2:n.456A>G
ENST00000557257.2:c.1118A>G	ENSP00000450578.2:p.Asp373Gly
ENST00000557555.3:c.1604A>G	ENSP00000451039.3:p.Asp535Gly
ENST00000686981.1:c.*1303A>G	ENSP00000510795.1:n.*1303A>G
ENST00000691052.1:c.*76A>G	ENSP00000508886.1:n.*76A>G
ENST00000691846.1:c.437A>G
ENST00000691973.1:c.1604A>G	ENSP00000509141.1:p.Asp535Gly
ENST00000257879.11:c.1592A>G MANE Select	ENSP00000257879.7:p.Asp531Gly
ENST00000553804.6:c.1604A>G	ENSP00000452120.1:p.Asp535Gly
ENST00000257879.10:c.1592A>G	ENSP00000257879.6:p.Asp531Gly
ENST00000347027.10:c.1574A>G	ENSP00000343009.6:p.Asp525Gly
ENST00000452168.6:c.1313A>G	ENSP00000393844.2:p.Asp438Gly
ENST00000553804.5:c.1604A>G	ENSP00000452120.1:p.Asp535Gly
ENST00000555728.5:c.1724A>G	ENSP00000452387.1:p.Asp575Gly
NM_001144996.1:c.1604A>G	NP_001138468.1:p.Asp535Gly
NM_001144997.1:c.1313A>G	NP_001138469.1:p.Asp438Gly
NM_002206.2:c.1592A>G	NP_002197.2:p.Asp531Gly
XM_005268839.1:c.1724A>G	XP_005268896.1:p.Asp575Gly
XM_005268840.1:c.1706A>G	XP_005268897.1:p.Asp569Gly
XM_005268841.1:c.1724A>G	XP_005268898.1:p.Asp575Gly
XM_005268842.1:c.1574A>G	XP_005268899.1:p.Asp525Gly
XM_005268844.1:c.1385A>G	XP_005268901.1:p.Asp462Gly
XM_005268845.1:c.1253A>G	XP_005268902.1:p.Asp418Gly
XM_005268846.1:c.1253A>G	XP_005268903.1:p.Asp418Gly
XM_005268847.1:c.1250A>G	XP_005268904.1:p.Asp417Gly
XM_005268848.1:c.1250A>G	XP_005268905.1:p.Asp417Gly
XM_005268849.1:c.1250A>G	XP_005268906.1:p.Asp417Gly
XM_005268850.1:c.1118A>G	XP_005268907.1:p.Asp373Gly
XM_011538286.1:c.1385A>G	XP_011536588.1:p.Asp462Gly
XM_011538287.1:c.1724A>G	XP_011536589.1:p.Asp575Gly
XM_005268839.2:c.1724A>G	XP_005268896.1:p.Asp575Gly
XM_005268840.2:c.1706A>G	XP_005268897.1:p.Asp569Gly
XM_005268841.2:c.1724A>G	XP_005268898.1:p.Asp575Gly
XM_005268842.2:c.1574A>G	XP_005268899.1:p.Asp525Gly
XM_017019265.1:c.1334A>G	XP_016874754.1:p.Asp445Gly
NM_001144996.2:c.1604A>G	NP_001138468.1:p.Asp535Gly
NM_001367993.1:c.1265A>G	NP_001354922.1:p.Asp422Gly
NM_001367994.1:c.248A>G	NP_001354923.1:p.Asp83Gly
NM_001374465.1:c.1574A>G	NP_001361394.1:p.Asp525Gly
NM_002206.3:c.1592A>G MANE Select	NP_002197.2:p.Asp531Gly