Canonical Allele Identifier: CA1314322269

Gene: ITGAV

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186633364T= , CM000664.2:g.186633364T=	GRCh38
NC_000002.11:g.187498091T= , CM000664.1:g.187498091T=	GRCh37
NC_000002.10:g.187206336T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696906.1:c.621T=	ENSP00000512967.1:p.Phe207=
ENST00000696907.1:c.444T=	ENSP00000512968.1:p.Phe148=
ENST00000696908.1:c.*31T=	ENSP00000512969.1:n.*31T=
ENST00000696909.1:c.444T=	ENSP00000512970.1:p.Phe148=
ENST00000696910.1:c.621T=	ENSP00000512971.1:p.Phe207=
ENST00000696911.1:c.621T=	ENSP00000512972.1:p.Phe207=
ENST00000696912.1:c.621T=	ENSP00000512973.1:p.Phe207=
ENST00000696913.1:c.621T=	ENSP00000512974.1:p.Phe207=
ENST00000696914.1:c.*173T=	ENSP00000512975.1:n.*173T=
ENST00000696917.1:n.1130T=
ENST00000696936.1:n.891T=
ENST00000696937.1:c.621T=	ENSP00000512982.1:p.Phe207=
ENST00000261023.8:c.621T= MANE Select	ENSP00000261023.3:p.Phe207=
ENST00000261023.7:c.621T=	ENSP00000261023.3:p.Phe207=
ENST00000374907.7:c.524-2718T=	ENSP00000364042.3:n.524-2718T=
ENST00000433736.6:c.483T=	ENSP00000404291.2:p.Phe161=
NM_001144999.2:c.483T=	NP_001138471.1:p.Phe161=
NM_001145000.2:c.524-2718T=	NP_001138472.1:n.524-2718T=
NM_002210.4:c.621T=	NP_002201.1:p.Phe207=
XM_006712513.2:c.180T=	XP_006712576.1:p.Phe60=
NM_002210.5:c.621T= MANE Select	NP_002201.2:p.Phe207=
NM_001145000.3:c.524-2718T=	NP_001138472.2:n.524-2718T=
NM_001144999.3:c.483T=	NP_001138471.2:p.Phe161=