Canonical Allele Identifier: CA8006345

Gene: ITGAL

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30489395T>G , CM000678.2:g.30489395T>G	GRCh38
NC_000016.9:g.30500716T>G , CM000678.1:g.30500716T>G	GRCh37
NC_000016.8:g.30408217T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002209.3:c.1213+9T>G MANE Select	NP_002200.2:n.1213+9T>G
ENST00000356798.11:c.1213+9T>G MANE Select	ENSP00000349252.5:n.1213+9T>G
NM_001114380.1:c.964+9T>G	NP_001107852.1:n.964+9T>G
NM_001114380.2:c.964+9T>G	NP_001107852.1:n.964+9T>G
NM_002209.2:c.1213+9T>G	NP_002200.2:n.1213+9T>G
ENST00000356798.10:c.1213+9T>G	ENSP00000349252.5:n.1213+9T>G
ENST00000358164.9:c.964+9T>G	ENSP00000350886.5:n.964+9T>G
ENST00000433423.2:c.154-9812T>G	ENSP00000409377.2:n.154-9812T>G
ENST00000564935.1:n.289+9T>G
ENST00000568012.5:n.180+240T>G
ENST00000568926.5:c.154-9978T>G	ENSP00000457785.1:n.154-9978T>G
ENST00000676652.1:c.896T>G
ENST00000677830.1:c.*279+9T>G	ENSP00000503623.1:n.*279+9T>G
ENST00000678203.1:c.*957+9T>G	ENSP00000504379.1:n.*957+9T>G
XM_005255313.1:c.1213+9T>G	XP_005255370.1:n.1213+9T>G
XM_006721044.1:c.964+9T>G	XP_006721107.1:n.964+9T>G
XM_011545849.1:c.925+9T>G	XP_011544151.1:n.925+9T>G
XM_024450262.1:c.925+9T>G	XP_024306030.1:n.925+9T>G
XR_950794.1:n.1309+9T>G