Canonical Allele Identifier: CA395578331

Gene: ITGAL

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30499211A>C , CM000678.2:g.30499211A>C	GRCh38
NC_000016.9:g.30510532A>C , CM000678.1:g.30510532A>C	GRCh37
NC_000016.8:g.30418033A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002209.3:c.1970A>C MANE Select	NP_002200.2:p.Lys657Thr
ENST00000356798.11:c.1970A>C MANE Select	ENSP00000349252.5:p.Lys657Thr
NM_001114380.1:c.1721A>C	NP_001107852.1:p.Lys574Thr
NM_001114380.2:c.1721A>C	NP_001107852.1:p.Lys574Thr
NM_002209.2:c.1970A>C	NP_002200.2:p.Lys657Thr
ENST00000356798.10:c.1970A>C	ENSP00000349252.5:p.Lys657Thr
ENST00000358164.9:c.1721A>C	ENSP00000350886.5:p.Lys574Thr
ENST00000433423.2:c.158A>C	ENSP00000409377.2:p.Lys53Thr
ENST00000563615.5:c.40A>C
ENST00000568926.5:c.154-162A>C	ENSP00000457785.1:n.154-162A>C
ENST00000568987.1:n.226A>C
ENST00000676652.1:c.4468A>C
ENST00000677830.1:c.*1036A>C	ENSP00000503623.1:n.*1036A>C
ENST00000678203.1:c.*1714A>C	ENSP00000504379.1:n.*1714A>C
XM_005255313.1:c.1970A>C	XP_005255370.1:p.Lys657Thr
XM_006721044.1:c.1721A>C	XP_006721107.1:p.Lys574Thr
XM_011545849.1:c.1682A>C	XP_011544151.1:p.Lys561Thr
XM_024450262.1:c.1682A>C	XP_024306030.1:p.Lys561Thr
XR_950794.1:n.2066A>C