Canonical Allele Identifier: CA385194155

Gene: ITGA7

Linked Data

• MyVariant Identifiers: chr12:g.56101330C>A (hg19) ; chr12:g.55707546C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55707546C>A , CM000674.2:g.55707546C>A	GRCh38
NC_000012.11:g.56101330C>A , CM000674.1:g.56101330C>A	GRCh37
NC_000012.10:g.54387597C>A	NCBI36
NG_012343.1:g.9760G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553893.6:c.65-4368G>T	ENSP00000452467.1:n.65-4368G>T
ENST00000557257.2:c.-61+4517G>T	ENSP00000450578.2:n.-61+4517G>T
ENST00000557555.3:c.137G>T	ENSP00000451039.3:p.Gly46Val
ENST00000686981.1:c.65-4368G>T	ENSP00000510795.1:n.65-4368G>T
ENST00000691052.1:c.137G>T	ENSP00000508886.1:p.Gly46Val
ENST00000691973.1:c.137G>T	ENSP00000509141.1:p.Gly46Val
ENST00000257879.11:c.137G>T MANE Select	ENSP00000257879.7:p.Gly46Val
ENST00000553804.6:c.137G>T	ENSP00000452120.1:p.Gly46Val
ENST00000257879.10:c.137G>T	ENSP00000257879.6:p.Gly46Val
ENST00000347027.10:c.137G>T	ENSP00000343009.6:p.Gly46Val
ENST00000452168.6:c.85+4517G>T	ENSP00000393844.2:n.85+4517G>T
ENST00000553276.1:n.142+4517G>T
ENST00000553737.5:n.191+4517G>T
ENST00000553804.5:c.137G>T	ENSP00000452120.1:p.Gly46Val
ENST00000553893.5:c.65-4368G>T	ENSP00000452467.1:n.65-4368G>T
ENST00000554359.1:n.168G>T
ENST00000554724.5:c.24-4368G>T
ENST00000555687.5:c.86-4368G>T	ENSP00000451311.1:n.86-4368G>T
ENST00000555728.5:c.137G>T	ENSP00000452387.1:p.Gly46Val
ENST00000555809.1:c.65-4368G>T	ENSP00000450798.1:n.65-4368G>T
ENST00000556273.5:c.64+4517G>T	ENSP00000450679.1:n.64+4517G>T
ENST00000556371.1:n.121+4517G>T
ENST00000557257.1:c.-61+4517G>T	ENSP00000450578.1:n.-61+4517G>T
NM_001144996.1:c.137G>T	NP_001138468.1:p.Gly46Val
NM_001144997.1:c.85+4517G>T	NP_001138469.1:n.85+4517G>T
NM_002206.2:c.137G>T	NP_002197.2:p.Gly46Val
XM_005268839.1:c.137G>T	XP_005268896.1:p.Gly46Val
XM_005268840.1:c.137G>T	XP_005268897.1:p.Gly46Val
XM_005268841.1:c.137G>T	XP_005268898.1:p.Gly46Val
XM_005268842.1:c.137G>T	XP_005268899.1:p.Gly46Val
XM_005268844.1:c.-133-4368G>T	XP_005268901.1:n.-133-4368G>T
XM_005268845.1:c.-133-4368G>T	XP_005268902.1:n.-133-4368G>T
XM_005268846.1:c.-133-4368G>T	XP_005268903.1:n.-133-4368G>T
XM_005268847.1:c.-61+4517G>T	XP_005268904.1:n.-61+4517G>T
XM_005268848.1:c.-61+4517G>T	XP_005268905.1:n.-61+4517G>T
XM_005268849.1:c.-61+4517G>T	XP_005268906.1:n.-61+4517G>T
XM_005268850.1:c.-61+4517G>T	XP_005268907.1:n.-61+4517G>T
XM_011538286.1:c.-133-4368G>T	XP_011536588.1:n.-133-4368G>T
XM_011538287.1:c.137G>T	XP_011536589.1:p.Gly46Val
XM_005268839.2:c.137G>T	XP_005268896.1:p.Gly46Val
XM_005268840.2:c.137G>T	XP_005268897.1:p.Gly46Val
XM_005268841.2:c.137G>T	XP_005268898.1:p.Gly46Val
XM_005268842.2:c.137G>T	XP_005268899.1:p.Gly46Val
NM_001144996.2:c.137G>T	NP_001138468.1:p.Gly46Val
NM_001367993.1:c.-133-4368G>T	NP_001354922.1:n.-133-4368G>T
NM_001367994.1:c.-1036G>T	NP_001354923.1:n.-1036G>T
NM_001374465.1:c.137G>T	NP_001361394.1:p.Gly46Val
NM_002206.3:c.137G>T MANE Select	NP_002197.2:p.Gly46Val