Canonical Allele Identifier: CA1040263203

Gene: ITGAV

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186678500G>A , CM000664.2:g.186678500G>A	GRCh38
NC_000002.11:g.187543227G>A , CM000664.1:g.187543227G>A	GRCh37
NC_000002.10:g.187251472G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696906.1:c.3124+1231G>A	ENSP00000512967.1:n.3124+1231G>A
ENST00000696907.1:c.*1208G>A	ENSP00000512968.1:n.*1208G>A
ENST00000696908.1:c.*3765G>A	ENSP00000512969.1:n.*3765G>A
ENST00000696909.1:c.*1208G>A	ENSP00000512970.1:n.*1208G>A
ENST00000696910.1:c.*1208G>A	ENSP00000512971.1:n.*1208G>A
ENST00000696911.1:c.*1208G>A	ENSP00000512972.1:n.*1208G>A
ENST00000696912.1:c.*1208G>A	ENSP00000512973.1:n.*1208G>A
ENST00000696913.1:c.*1208G>A	ENSP00000512974.1:n.*1208G>A
ENST00000696914.1:c.*3907G>A	ENSP00000512975.1:n.*3907G>A
ENST00000696917.1:n.4886G>A
ENST00000696918.1:n.5562G>A
ENST00000696919.1:n.5538G>A
ENST00000696937.1:c.*2025G>A	ENSP00000512982.1:n.*2025G>A
ENST00000261023.8:c.*1208G>A MANE Select	ENSP00000261023.3:n.*1208G>A
ENST00000261023.7:c.*1208G>A	ENSP00000261023.3:n.*1208G>A
ENST00000374907.7:c.*1208G>A	ENSP00000364042.3:n.*1208G>A
NM_001144999.2:c.*1208G>A	NP_001138471.1:n.*1208G>A
NM_001145000.2:c.*1208G>A	NP_001138472.1:n.*1208G>A
NM_002210.4:c.*1208G>A	NP_002201.1:n.*1208G>A
XM_006712513.2:c.*1208G>A	XP_006712576.1:n.*1208G>A
NM_002210.5:c.*1208G>A MANE Select	NP_002201.2:n.*1208G>A
NM_001145000.3:c.*1208G>A	NP_001138472.2:n.*1208G>A
NM_001144999.3:c.*1208G>A	NP_001138471.2:n.*1208G>A