Canonical Allele Identifier: CA1314338458

Gene: ITGAV

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186669014T>G , CM000664.2:g.186669014T>G	GRCh38
NC_000002.11:g.187533741T>G , CM000664.1:g.187533741T>G	GRCh37
NC_000002.10:g.187241986T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496854.2:n.397+94T>G
ENST00000696906.1:c.2592+94T>G	ENSP00000512967.1:n.2592+94T>G
ENST00000696907.1:c.2307+94T>G	ENSP00000512968.1:n.2307+94T>G
ENST00000696908.1:c.*2002+94T>G	ENSP00000512969.1:n.*2002+94T>G
ENST00000696909.1:c.2415+94T>G	ENSP00000512970.1:n.2415+94T>G
ENST00000696910.1:c.2592+94T>G	ENSP00000512971.1:n.2592+94T>G
ENST00000696911.1:c.2592+94T>G	ENSP00000512972.1:n.2592+94T>G
ENST00000696912.1:c.2484+94T>G	ENSP00000512973.1:n.2484+94T>G
ENST00000696913.1:c.2511+94T>G	ENSP00000512974.1:n.2511+94T>G
ENST00000696914.1:c.*2144+94T>G	ENSP00000512975.1:n.*2144+94T>G
ENST00000696917.1:n.3123+94T>G
ENST00000696918.1:n.3538+94T>G
ENST00000696937.1:c.*262+94T>G	ENSP00000512982.1:n.*262+94T>G
ENST00000261023.8:c.2592+94T>G MANE Select	ENSP00000261023.3:n.2592+94T>G
ENST00000261023.7:c.2592+94T>G	ENSP00000261023.3:n.2592+94T>G
ENST00000374907.7:c.2484+94T>G	ENSP00000364042.3:n.2484+94T>G
ENST00000430709.1:c.44+94T>G
ENST00000433736.6:c.2454+94T>G	ENSP00000404291.2:n.2454+94T>G
ENST00000474571.1:n.76+94T>G
ENST00000496477.1:n.288+94T>G
ENST00000496854.1:n.397+94T>G
NM_001144999.2:c.2454+94T>G	NP_001138471.1:n.2454+94T>G
NM_001145000.2:c.2484+94T>G	NP_001138472.1:n.2484+94T>G
NM_002210.4:c.2592+94T>G	NP_002201.1:n.2592+94T>G
XM_006712513.2:c.2151+94T>G	XP_006712576.1:n.2151+94T>G
NM_002210.5:c.2592+94T>G MANE Select	NP_002201.2:n.2592+94T>G
NM_001145000.3:c.2484+94T>G	NP_001138472.2:n.2484+94T>G
NM_001144999.3:c.2454+94T>G	NP_001138471.2:n.2454+94T>G