Canonical Allele Identifier: CA349976468

Gene: ITGAV

Linked Data

• MyVariant Identifiers: chr2:g.187498060A>T (hg19) ; chr2:g.186633333A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186633333A>T , CM000664.2:g.186633333A>T	GRCh38
NC_000002.11:g.187498060A>T , CM000664.1:g.187498060A>T	GRCh37
NC_000002.10:g.187206305A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696906.1:c.590A>T	ENSP00000512967.1:p.Asp197Val
ENST00000696907.1:c.413A>T	ENSP00000512968.1:p.Asp138Val
ENST00000696908.1:c.528A>T	ENSP00000512969.1:p.Ter176Cys
ENST00000696909.1:c.413A>T	ENSP00000512970.1:p.Asp138Val
ENST00000696910.1:c.590A>T	ENSP00000512971.1:p.Asp197Val
ENST00000696911.1:c.590A>T	ENSP00000512972.1:p.Asp197Val
ENST00000696912.1:c.590A>T	ENSP00000512973.1:p.Asp197Val
ENST00000696913.1:c.590A>T	ENSP00000512974.1:p.Asp197Val
ENST00000696914.1:c.*142A>T	ENSP00000512975.1:n.*142A>T
ENST00000696917.1:n.1099A>T
ENST00000696936.1:n.860A>T
ENST00000696937.1:c.590A>T	ENSP00000512982.1:p.Asp197Val
ENST00000261023.8:c.590A>T MANE Select	ENSP00000261023.3:p.Asp197Val
ENST00000261023.7:c.590A>T	ENSP00000261023.3:p.Asp197Val
ENST00000374907.7:c.524-2749A>T	ENSP00000364042.3:n.524-2749A>T
ENST00000433736.6:c.452A>T	ENSP00000404291.2:p.Asp151Val
NM_001144999.2:c.452A>T	NP_001138471.1:p.Asp151Val
NM_001145000.2:c.524-2749A>T	NP_001138472.1:n.524-2749A>T
NM_002210.4:c.590A>T	NP_002201.1:p.Asp197Val
XM_006712513.2:c.149A>T	XP_006712576.1:p.Asp50Val
NM_002210.5:c.590A>T MANE Select	NP_002201.2:p.Asp197Val
NM_001145000.3:c.524-2749A>T	NP_001138472.2:n.524-2749A>T
NM_001144999.3:c.452A>T	NP_001138471.2:p.Asp151Val