Canonical Allele Identifier: CA1314319906

Gene: ITGAV

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186628015G>C , CM000664.2:g.186628015G>C	GRCh38
NC_000002.11:g.187492742G>C , CM000664.1:g.187492742G>C	GRCh37
NC_000002.10:g.187200987G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696906.1:c.523+2428G>C	ENSP00000512967.1:n.523+2428G>C
ENST00000696907.1:c.409-5314G>C	ENSP00000512968.1:n.409-5314G>C
ENST00000696908.1:c.523+2428G>C	ENSP00000512969.1:n.523+2428G>C
ENST00000696909.1:c.409-5314G>C	ENSP00000512970.1:n.409-5314G>C
ENST00000696910.1:c.523+2428G>C	ENSP00000512971.1:n.523+2428G>C
ENST00000696911.1:c.523+2428G>C	ENSP00000512972.1:n.523+2428G>C
ENST00000696912.1:c.523+2428G>C	ENSP00000512973.1:n.523+2428G>C
ENST00000696913.1:c.523+2428G>C	ENSP00000512974.1:n.523+2428G>C
ENST00000696914.1:c.503+2448G>C	ENSP00000512975.1:n.503+2448G>C
ENST00000696936.1:n.793+2428G>C
ENST00000696937.1:c.523+2428G>C	ENSP00000512982.1:n.523+2428G>C
ENST00000261023.8:c.523+2428G>C MANE Select	ENSP00000261023.3:n.523+2428G>C
ENST00000261023.7:c.523+2428G>C	ENSP00000261023.3:n.523+2428G>C
ENST00000374907.7:c.523+2428G>C	ENSP00000364042.3:n.523+2428G>C
ENST00000433736.6:c.385+2428G>C	ENSP00000404291.2:n.385+2428G>C
NM_001144999.2:c.385+2428G>C	NP_001138471.1:n.385+2428G>C
NM_001145000.2:c.523+2428G>C	NP_001138472.1:n.523+2428G>C
NM_002210.4:c.523+2428G>C	NP_002201.1:n.523+2428G>C
XM_006712513.2:c.82+2428G>C	XP_006712576.1:n.82+2428G>C
NM_002210.5:c.523+2428G>C MANE Select	NP_002201.2:n.523+2428G>C
NM_001145000.3:c.523+2428G>C	NP_001138472.2:n.523+2428G>C
NM_001144999.3:c.385+2428G>C	NP_001138471.2:n.385+2428G>C