Canonical Allele Identifier: CA2018586

Gene: ITGAV

Linked Data

• dbSNP Id: rs762728962
• ExAC: 2:187498008 A / G
• gnomAD v2: 2-187498008-A-G
• gnomAD v3: 2-186633281-A-G
• gnomAD v4: 2-186633281-A-G
• MyVariant Identifiers: chr2:g.187498008A>G (hg19) ; chr2:g.186633281A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186633281A>G , CM000664.2:g.186633281A>G	GRCh38
NC_000002.11:g.187498008A>G , CM000664.1:g.187498008A>G	GRCh37
NC_000002.10:g.187206253A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696906.1:c.586-48A>G	ENSP00000512967.1:n.586-48A>G
ENST00000696907.1:c.409-48A>G	ENSP00000512968.1:n.409-48A>G
ENST00000696908.1:c.524-48A>G	ENSP00000512969.1:n.524-48A>G
ENST00000696909.1:c.409-48A>G	ENSP00000512970.1:n.409-48A>G
ENST00000696910.1:c.586-48A>G	ENSP00000512971.1:n.586-48A>G
ENST00000696911.1:c.586-48A>G	ENSP00000512972.1:n.586-48A>G
ENST00000696912.1:c.586-48A>G	ENSP00000512973.1:n.586-48A>G
ENST00000696913.1:c.586-48A>G	ENSP00000512974.1:n.586-48A>G
ENST00000696914.1:c.*138-48A>G	ENSP00000512975.1:n.*138-48A>G
ENST00000696917.1:n.1095-48A>G
ENST00000696936.1:n.856-48A>G
ENST00000696937.1:c.586-48A>G	ENSP00000512982.1:n.586-48A>G
ENST00000261023.8:c.586-48A>G MANE Select	ENSP00000261023.3:n.586-48A>G
ENST00000261023.7:c.586-48A>G	ENSP00000261023.3:n.586-48A>G
ENST00000374907.7:c.524-2801A>G	ENSP00000364042.3:n.524-2801A>G
ENST00000433736.6:c.448-48A>G	ENSP00000404291.2:n.448-48A>G
NM_001144999.2:c.448-48A>G	NP_001138471.1:n.448-48A>G
NM_001145000.2:c.524-2801A>G	NP_001138472.1:n.524-2801A>G
NM_002210.4:c.586-48A>G	NP_002201.1:n.586-48A>G
XM_006712513.2:c.145-48A>G	XP_006712576.1:n.145-48A>G
NM_002210.5:c.586-48A>G MANE Select	NP_002201.2:n.586-48A>G
NM_001145000.3:c.524-2801A>G	NP_001138472.2:n.524-2801A>G
NM_001144999.3:c.448-48A>G	NP_001138471.2:n.448-48A>G