Canonical Allele Identifier: CA8006524

Gene: ITGAL

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30496559G>A , CM000678.2:g.30496559G>A	GRCh38
NC_000016.9:g.30507880G>A , CM000678.1:g.30507880G>A	GRCh37
NC_000016.8:g.30415381G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002209.3:c.1825G>A MANE Select	NP_002200.2:p.Val609Met
ENST00000356798.11:c.1825G>A MANE Select	ENSP00000349252.5:p.Val609Met
NM_001114380.1:c.1576G>A	NP_001107852.1:p.Val526Met
NM_001114380.2:c.1576G>A	NP_001107852.1:p.Val526Met
NM_002209.2:c.1825G>A	NP_002200.2:p.Val609Met
ENST00000356798.10:c.1825G>A	ENSP00000349252.5:p.Val609Met
ENST00000358164.9:c.1576G>A	ENSP00000350886.5:p.Val526Met
ENST00000433423.2:c.154-2648G>A	ENSP00000409377.2:n.154-2648G>A
ENST00000568926.5:c.154-2814G>A	ENSP00000457785.1:n.154-2814G>A
ENST00000568987.1:n.128G>A
ENST00000676652.1:c.4323G>A
ENST00000677830.1:c.*891G>A	ENSP00000503623.1:n.*891G>A
ENST00000678203.1:c.*1569G>A	ENSP00000504379.1:n.*1569G>A
XM_005255313.1:c.1825G>A	XP_005255370.1:p.Val609Met
XM_006721044.1:c.1576G>A	XP_006721107.1:p.Val526Met
XM_011545849.1:c.1537G>A	XP_011544151.1:p.Val513Met
XM_024450262.1:c.1537G>A	XP_024306030.1:p.Val513Met
XR_950794.1:n.1921G>A