Canonical Allele Identifier: CA349976556

Gene: ITGAV

Linked Data

• MyVariant Identifiers: chr2:g.187498100A>C (hg19) ; chr2:g.186633373A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186633373A>C , CM000664.2:g.186633373A>C	GRCh38
NC_000002.11:g.187498100A>C , CM000664.1:g.187498100A>C	GRCh37
NC_000002.10:g.187206345A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696906.1:c.630A>C	ENSP00000512967.1:p.Gln210His
ENST00000696907.1:c.453A>C	ENSP00000512968.1:p.Gln151His
ENST00000696908.1:c.*40A>C	ENSP00000512969.1:n.*40A>C
ENST00000696909.1:c.453A>C	ENSP00000512970.1:p.Gln151His
ENST00000696910.1:c.630A>C	ENSP00000512971.1:p.Gln210His
ENST00000696911.1:c.630A>C	ENSP00000512972.1:p.Gln210His
ENST00000696912.1:c.630A>C	ENSP00000512973.1:p.Gln210His
ENST00000696913.1:c.630A>C	ENSP00000512974.1:p.Gln210His
ENST00000696914.1:c.*182A>C	ENSP00000512975.1:n.*182A>C
ENST00000696917.1:n.1139A>C
ENST00000696936.1:n.900A>C
ENST00000696937.1:c.630A>C	ENSP00000512982.1:p.Gln210His
ENST00000261023.8:c.630A>C MANE Select	ENSP00000261023.3:p.Gln210His
ENST00000261023.7:c.630A>C	ENSP00000261023.3:p.Gln210His
ENST00000374907.7:c.524-2709A>C	ENSP00000364042.3:n.524-2709A>C
ENST00000433736.6:c.492A>C	ENSP00000404291.2:p.Gln164His
NM_001144999.2:c.492A>C	NP_001138471.1:p.Gln164His
NM_001145000.2:c.524-2709A>C	NP_001138472.1:n.524-2709A>C
NM_002210.4:c.630A>C	NP_002201.1:p.Gln210His
XM_006712513.2:c.189A>C	XP_006712576.1:p.Gln63His
NM_002210.5:c.630A>C MANE Select	NP_002201.2:p.Gln210His
NM_001145000.3:c.524-2709A>C	NP_001138472.2:n.524-2709A>C
NM_001144999.3:c.492A>C	NP_001138471.2:p.Gln164His