Canonical Allele Identifier: CA916731109

Gene: ITGAV

Linked Data

• dbSNP Id: rs1559051317

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186633394dup , CM000664.2:g.186633394dup	GRCh38
NC_000002.11:g.187498121dup , CM000664.1:g.187498121dup	GRCh37
NC_000002.10:g.187206366dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696906.1:c.631+20dup	ENSP00000512967.1:n.631+20dup
ENST00000696907.1:c.454+20dup	ENSP00000512968.1:n.454+20dup
ENST00000696908.1:c.*41+20dup	ENSP00000512969.1:n.*41+20dup
ENST00000696909.1:c.454+20dup	ENSP00000512970.1:n.454+20dup
ENST00000696910.1:c.631+20dup	ENSP00000512971.1:n.631+20dup
ENST00000696911.1:c.631+20dup	ENSP00000512972.1:n.631+20dup
ENST00000696912.1:c.631+20dup	ENSP00000512973.1:n.631+20dup
ENST00000696913.1:c.631+20dup	ENSP00000512974.1:n.631+20dup
ENST00000696914.1:c.*183+20dup	ENSP00000512975.1:n.*183+20dup
ENST00000696917.1:n.1140+20dup
ENST00000696936.1:n.901+20dup
ENST00000696937.1:c.631+20dup	ENSP00000512982.1:n.631+20dup
ENST00000261023.8:c.631+20dup MANE Select	ENSP00000261023.3:n.631+20dup
ENST00000261023.7:c.631+20dup	ENSP00000261023.3:n.631+20dup
ENST00000374907.7:c.524-2688dup	ENSP00000364042.3:n.524-2688dup
ENST00000433736.6:c.493+20dup	ENSP00000404291.2:n.493+20dup
NM_001144999.2:c.493+20dup	NP_001138471.1:n.493+20dup
NM_001145000.2:c.524-2688dup	NP_001138472.1:n.524-2688dup
NM_002210.4:c.631+20dup	NP_002201.1:n.631+20dup
XM_006712513.2:c.190+20dup	XP_006712576.1:n.190+20dup
NM_002210.5:c.631+20dup MANE Select	NP_002201.2:n.631+20dup
NM_001145000.3:c.524-2688dup	NP_001138472.2:n.524-2688dup
NM_001144999.3:c.493+20dup	NP_001138471.2:n.493+20dup