Canonical Allele Identifier: CA2662275733

Gene: ITGAV

Linked Data

• gnomAD v4: 2-186633295-A-AAT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186633302_186633303dup , CM000664.2:g.186633302_186633303dup	GRCh38
NC_000002.11:g.187498029_187498030dup , CM000664.1:g.187498029_187498030dup	GRCh37
NC_000002.10:g.187206274_187206275dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000696906.1:c.586-27_586-26dup	ENSP00000512967.1:n.586-27_586-26dup
ENST00000696907.1:c.409-27_409-26dup	ENSP00000512968.1:n.409-27_409-26dup
ENST00000696908.1:c.524-27_524-26dup	ENSP00000512969.1:n.524-27_524-26dup
ENST00000696909.1:c.409-27_409-26dup	ENSP00000512970.1:n.409-27_409-26dup
ENST00000696910.1:c.586-27_586-26dup	ENSP00000512971.1:n.586-27_586-26dup
ENST00000696911.1:c.586-27_586-26dup	ENSP00000512972.1:n.586-27_586-26dup
ENST00000696912.1:c.586-27_586-26dup	ENSP00000512973.1:n.586-27_586-26dup
ENST00000696913.1:c.586-27_586-26dup	ENSP00000512974.1:n.586-27_586-26dup
ENST00000696914.1:c.*138-27_*138-26dup	ENSP00000512975.1:n.*138-27_*138-26dup
ENST00000696917.1:n.1095-27_1095-26dup
ENST00000696936.1:n.856-27_856-26dup
ENST00000696937.1:c.586-27_586-26dup	ENSP00000512982.1:n.586-27_586-26dup
ENST00000261023.8:c.586-27_586-26dup MANE Select	ENSP00000261023.3:n.586-27_586-26dup
ENST00000261023.7:c.586-27_586-26dup	ENSP00000261023.3:n.586-27_586-26dup
ENST00000374907.7:c.524-2780_524-2779dup	ENSP00000364042.3:n.524-2780_524-2779dup
ENST00000433736.6:c.448-27_448-26dup	ENSP00000404291.2:n.448-27_448-26dup
NM_001144999.2:c.448-27_448-26dup	NP_001138471.1:n.448-27_448-26dup
NM_001145000.2:c.524-2780_524-2779dup	NP_001138472.1:n.524-2780_524-2779dup
NM_002210.4:c.586-27_586-26dup	NP_002201.1:n.586-27_586-26dup
XM_006712513.2:c.145-27_145-26dup	XP_006712576.1:n.145-27_145-26dup
NM_002210.5:c.586-27_586-26dup MANE Select	NP_002201.2:n.586-27_586-26dup
NM_001145000.3:c.524-2780_524-2779dup	NP_001138472.2:n.524-2780_524-2779dup
NM_001144999.3:c.448-27_448-26dup	NP_001138471.2:n.448-27_448-26dup