Canonical Allele Identifier: CA395564164

Gene: ITGAL

Linked Data

• MyVariant Identifiers: chr16:g.30492831C>G (hg19) ; chr16:g.30481510C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30481510C>G , CM000678.2:g.30481510C>G	GRCh38
NC_000016.9:g.30492831C>G , CM000678.1:g.30492831C>G	GRCh37
NC_000016.8:g.30400332C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356798.11:c.648C>G MANE Select	ENSP00000349252.5:p.Asp216Glu
ENST00000676652.1:c.322C>G
ENST00000677830.1:c.399C>G	ENSP00000503623.1:p.Asp133Glu
ENST00000678203.1:c.*392C>G	ENSP00000504379.1:n.*392C>G
ENST00000356798.10:c.648C>G	ENSP00000349252.5:p.Asp216Glu
ENST00000358164.9:c.399C>G	ENSP00000350886.5:p.Asp133Glu
ENST00000433423.2:c.153+7223C>G	ENSP00000409377.2:n.153+7223C>G
ENST00000562857.5:c.*28C>G	ENSP00000454342.1:n.*28C>G
ENST00000564118.1:c.399C>G	ENSP00000456888.1:p.Asp133Glu
ENST00000565348.5:n.420-2317C>G
ENST00000568926.5:c.153+7223C>G	ENSP00000457785.1:n.153+7223C>G
NM_001114380.1:c.399C>G	NP_001107852.1:p.Asp133Glu
NM_002209.2:c.648C>G	NP_002200.2:p.Asp216Glu
XM_005255313.1:c.648C>G	XP_005255370.1:p.Asp216Glu
XM_006721044.1:c.399C>G	XP_006721107.1:p.Asp133Glu
XM_011545849.1:c.360C>G	XP_011544151.1:p.Asp120Glu
XR_950794.1:n.744C>G
XM_024450262.1:c.360C>G	XP_024306030.1:p.Asp120Glu
NM_001114380.2:c.399C>G	NP_001107852.1:p.Asp133Glu
NM_002209.3:c.648C>G MANE Select	NP_002200.2:p.Asp216Glu