Canonical Allele Identifier: CA2216594213

Gene: ITGAL

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30505171A>C , CM000678.2:g.30505171A>C	GRCh38
NC_000016.9:g.30516492A>C , CM000678.1:g.30516492A>C	GRCh37
NC_000016.8:g.30423993A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356798.11:c.2236-73A>C MANE Select	ENSP00000349252.5:n.2236-73A>C
ENST00000676652.1:c.4734-76A>C
ENST00000677830.1:c.*1302-73A>C	ENSP00000503623.1:n.*1302-73A>C
ENST00000678203.1:c.*1980-76A>C	ENSP00000504379.1:n.*1980-76A>C
ENST00000356798.10:c.2236-73A>C	ENSP00000349252.5:n.2236-73A>C
ENST00000358164.9:c.1987-76A>C	ENSP00000350886.5:n.1987-76A>C
ENST00000433423.2:c.333+5682A>C	ENSP00000409377.2:n.333+5682A>C
ENST00000562020.1:n.300A>C
ENST00000563615.5:c.271-76A>C
ENST00000568926.5:c.271-1544A>C	ENSP00000457785.1:n.271-1544A>C
NM_001114380.1:c.1987-76A>C	NP_001107852.1:n.1987-76A>C
NM_002209.2:c.2236-73A>C	NP_002200.2:n.2236-73A>C
XM_005255313.1:c.2236-76A>C	XP_005255370.1:n.2236-76A>C
XM_006721044.1:c.1987-73A>C	XP_006721107.1:n.1987-73A>C
XM_011545849.1:c.1948-73A>C	XP_011544151.1:n.1948-73A>C
XR_950794.1:n.2297-76A>C
XM_024450262.1:c.1948-73A>C	XP_024306030.1:n.1948-73A>C
NM_001114380.2:c.1987-76A>C	NP_001107852.1:n.1987-76A>C
NM_002209.3:c.2236-73A>C MANE Select	NP_002200.2:n.2236-73A>C