Canonical Allele Identifier: CA395558298

Gene: ITGAL

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30474235G>A , CM000678.2:g.30474235G>A	GRCh38
NC_000016.9:g.30485556G>A , CM000678.1:g.30485556G>A	GRCh37
NC_000016.8:g.30393057G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002209.3:c.101G>A MANE Select	NP_002200.2:p.Arg34Gln
ENST00000356798.11:c.101G>A MANE Select	ENSP00000349252.5:p.Arg34Gln
NM_001114380.1:c.101G>A	NP_001107852.1:p.Arg34Gln
NM_001114380.2:c.101G>A	NP_001107852.1:p.Arg34Gln
NM_002209.2:c.101G>A	NP_002200.2:p.Arg34Gln
ENST00000356798.10:c.101G>A	ENSP00000349252.5:p.Arg34Gln
ENST00000358164.9:c.101G>A	ENSP00000350886.5:p.Arg34Gln
ENST00000433423.2:c.101G>A	ENSP00000409377.2:p.Arg34Gln
ENST00000562652.1:c.*59G>A	ENSP00000456521.1:n.*59G>A
ENST00000562857.5:c.101G>A	ENSP00000454342.1:p.Arg34Gln
ENST00000564118.1:c.101G>A	ENSP00000456888.1:p.Arg34Gln
ENST00000565348.5:n.193G>A
ENST00000565864.5:c.101G>A	ENSP00000454908.1:p.Arg34Gln
ENST00000568926.5:c.101G>A	ENSP00000457785.1:p.Arg34Gln
ENST00000569570.5:n.336G>A
ENST00000569725.1:c.-188G>A	ENSP00000461006.1:n.-188G>A
ENST00000677830.1:c.101G>A	ENSP00000503623.1:p.Arg34Gln
ENST00000678203.1:c.220G>A	ENSP00000504379.1:p.Gly74Arg
XM_005255313.1:c.101G>A	XP_005255370.1:p.Arg34Gln
XM_006721044.1:c.101G>A	XP_006721107.1:p.Arg34Gln
XM_011545849.1:c.-205G>A	XP_011544151.1:n.-205G>A
XM_024450262.1:c.-188G>A	XP_024306030.1:n.-188G>A
XR_950794.1:n.197G>A