Canonical Allele Identifier: CA1314345486

Gene: ITGAV

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186678647C= , CM000664.2:g.186678647C=	GRCh38
NC_000002.11:g.187543374C= , CM000664.1:g.187543374C=	GRCh37
NC_000002.10:g.187251619C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696906.1:c.3124+1378C=	ENSP00000512967.1:n.3124+1378C=
ENST00000696907.1:c.*1355C=	ENSP00000512968.1:n.*1355C=
ENST00000696908.1:c.*3912C=	ENSP00000512969.1:n.*3912C=
ENST00000696909.1:c.*1355C=	ENSP00000512970.1:n.*1355C=
ENST00000696910.1:c.*1355C=	ENSP00000512971.1:n.*1355C=
ENST00000696911.1:c.*1355C=	ENSP00000512972.1:n.*1355C=
ENST00000696912.1:c.*1355C=	ENSP00000512973.1:n.*1355C=
ENST00000696913.1:c.*1355C=	ENSP00000512974.1:n.*1355C=
ENST00000696914.1:c.*4054C=	ENSP00000512975.1:n.*4054C=
ENST00000696917.1:n.5033C=
ENST00000696918.1:n.5709C=
ENST00000696919.1:n.5685C=
ENST00000696937.1:c.*2172C=	ENSP00000512982.1:n.*2172C=
ENST00000261023.8:c.*1355C= MANE Select	ENSP00000261023.3:n.*1355C=
ENST00000261023.7:c.*1355C=	ENSP00000261023.3:n.*1355C=
ENST00000374907.7:c.*1355C=	ENSP00000364042.3:n.*1355C=
NM_001144999.2:c.*1355C=	NP_001138471.1:n.*1355C=
NM_001145000.2:c.*1355C=	NP_001138472.1:n.*1355C=
NM_002210.4:c.*1355C=	NP_002201.1:n.*1355C=
XM_006712513.2:c.*1355C=	XP_006712576.1:n.*1355C=
NM_002210.5:c.*1355C= MANE Select	NP_002201.2:n.*1355C=
NM_001145000.3:c.*1355C=	NP_001138472.2:n.*1355C=
NM_001144999.3:c.*1355C=	NP_001138471.2:n.*1355C=