Canonical Allele Identifier: CA2577183092

Gene: ITGAV

Linked Data

• gnomAD v4: 2-186633275-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186633280_186633281del , CM000664.2:g.186633280_186633281del	GRCh38
NC_000002.11:g.187498007_187498008del , CM000664.1:g.187498007_187498008del	GRCh37
NC_000002.10:g.187206252_187206253del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696906.1:c.586-49_586-48del	ENSP00000512967.1:n.586-49_586-48del
ENST00000696907.1:c.409-49_409-48del	ENSP00000512968.1:n.409-49_409-48del
ENST00000696908.1:c.524-49_524-48del	ENSP00000512969.1:n.524-49_524-48del
ENST00000696909.1:c.409-49_409-48del	ENSP00000512970.1:n.409-49_409-48del
ENST00000696910.1:c.586-49_586-48del	ENSP00000512971.1:n.586-49_586-48del
ENST00000696911.1:c.586-49_586-48del	ENSP00000512972.1:n.586-49_586-48del
ENST00000696912.1:c.586-49_586-48del	ENSP00000512973.1:n.586-49_586-48del
ENST00000696913.1:c.586-49_586-48del	ENSP00000512974.1:n.586-49_586-48del
ENST00000696914.1:c.*138-49_*138-48del	ENSP00000512975.1:n.*138-49_*138-48del
ENST00000696917.1:n.1095-49_1095-48del
ENST00000696936.1:n.856-49_856-48del
ENST00000696937.1:c.586-49_586-48del	ENSP00000512982.1:n.586-49_586-48del
ENST00000261023.8:c.586-49_586-48del MANE Select	ENSP00000261023.3:n.586-49_586-48del
ENST00000261023.7:c.586-49_586-48del	ENSP00000261023.3:n.586-49_586-48del
ENST00000374907.7:c.524-2802_524-2801del	ENSP00000364042.3:n.524-2802_524-2801del
ENST00000433736.6:c.448-49_448-48del	ENSP00000404291.2:n.448-49_448-48del
NM_001144999.2:c.448-49_448-48del	NP_001138471.1:n.448-49_448-48del
NM_001145000.2:c.524-2802_524-2801del	NP_001138472.1:n.524-2802_524-2801del
NM_002210.4:c.586-49_586-48del	NP_002201.1:n.586-49_586-48del
XM_006712513.2:c.145-49_145-48del	XP_006712576.1:n.145-49_145-48del
NM_002210.5:c.586-49_586-48del MANE Select	NP_002201.2:n.586-49_586-48del
NM_001145000.3:c.524-2802_524-2801del	NP_001138472.2:n.524-2802_524-2801del
NM_001144999.3:c.448-49_448-48del	NP_001138471.2:n.448-49_448-48del