Canonical Allele Identifier: CA1314322259

Gene: ITGAV

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186633349T= , CM000664.2:g.186633349T=	GRCh38
NC_000002.11:g.187498076T= , CM000664.1:g.187498076T=	GRCh37
NC_000002.10:g.187206321T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696906.1:c.606T=	ENSP00000512967.1:p.Gly202=
ENST00000696907.1:c.429T=	ENSP00000512968.1:p.Gly143=
ENST00000696908.1:c.*16T=	ENSP00000512969.1:n.*16T=
ENST00000696909.1:c.429T=	ENSP00000512970.1:p.Gly143=
ENST00000696910.1:c.606T=	ENSP00000512971.1:p.Gly202=
ENST00000696911.1:c.606T=	ENSP00000512972.1:p.Gly202=
ENST00000696912.1:c.606T=	ENSP00000512973.1:p.Gly202=
ENST00000696913.1:c.606T=	ENSP00000512974.1:p.Gly202=
ENST00000696914.1:c.*158T=	ENSP00000512975.1:n.*158T=
ENST00000696917.1:n.1115T=
ENST00000696936.1:n.876T=
ENST00000696937.1:c.606T=	ENSP00000512982.1:p.Gly202=
ENST00000261023.8:c.606T= MANE Select	ENSP00000261023.3:p.Gly202=
ENST00000261023.7:c.606T=	ENSP00000261023.3:p.Gly202=
ENST00000374907.7:c.524-2733T=	ENSP00000364042.3:n.524-2733T=
ENST00000433736.6:c.468T=	ENSP00000404291.2:p.Gly156=
NM_001144999.2:c.468T=	NP_001138471.1:p.Gly156=
NM_001145000.2:c.524-2733T=	NP_001138472.1:n.524-2733T=
NM_002210.4:c.606T=	NP_002201.1:p.Gly202=
XM_006712513.2:c.165T=	XP_006712576.1:p.Gly55=
NM_002210.5:c.606T= MANE Select	NP_002201.2:p.Gly202=
NM_001145000.3:c.524-2733T=	NP_001138472.2:n.524-2733T=
NM_001144999.3:c.468T=	NP_001138471.2:p.Gly156=