Canonical Allele Identifier: CA1314322367

Gene: ITGAV

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.186633583_186633585delinsCTG , CM000664.2:g.186633583_186633585delinsCTG	GRCh38
NC_000002.11:g.187498310_187498312delinsCTG , CM000664.1:g.187498310_187498312delinsCTG	GRCh37
NC_000002.10:g.187206555_187206557delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696906.1:c.631+209_631+211delinsCTG	ENSP00000512967.1:n.631+209_631+211delinsCTG
ENST00000696907.1:c.454+209_454+211delinsCTG	ENSP00000512968.1:n.454+209_454+211delinsCTG
ENST00000696908.1:c.*41+209_*41+211delinsCTG	ENSP00000512969.1:n.*41+209_*41+211delinsCTG
ENST00000696909.1:c.454+209_454+211delinsCTG	ENSP00000512970.1:n.454+209_454+211delinsCTG
ENST00000696910.1:c.631+209_631+211delinsCTG	ENSP00000512971.1:n.631+209_631+211delinsCTG
ENST00000696911.1:c.631+209_631+211delinsCTG	ENSP00000512972.1:n.631+209_631+211delinsCTG
ENST00000696912.1:c.631+209_631+211delinsCTG	ENSP00000512973.1:n.631+209_631+211delinsCTG
ENST00000696913.1:c.631+209_631+211delinsCTG	ENSP00000512974.1:n.631+209_631+211delinsCTG
ENST00000696914.1:c.*183+209_*183+211delinsCTG	ENSP00000512975.1:n.*183+209_*183+211delinsCTG
ENST00000696917.1:n.1140+209_1140+211delinsCTG
ENST00000696936.1:n.901+209_901+211delinsCTG
ENST00000696937.1:c.631+209_631+211delinsCTG	ENSP00000512982.1:n.631+209_631+211delinsCTG
ENST00000261023.8:c.631+209_631+211delinsCTG MANE Select	ENSP00000261023.3:n.631+209_631+211delinsCTG
ENST00000261023.7:c.631+209_631+211delinsCTG	ENSP00000261023.3:n.631+209_631+211delinsCTG
ENST00000374907.7:c.524-2499_524-2497delinsCTG	ENSP00000364042.3:n.524-2499_524-2497delinsCTG
ENST00000433736.6:c.493+209_493+211delinsCTG	ENSP00000404291.2:n.493+209_493+211delinsCTG
NM_001144999.2:c.493+209_493+211delinsCTG	NP_001138471.1:n.493+209_493+211delinsCTG
NM_001145000.2:c.524-2499_524-2497delinsCTG	NP_001138472.1:n.524-2499_524-2497delinsCTG
NM_002210.4:c.631+209_631+211delinsCTG	NP_002201.1:n.631+209_631+211delinsCTG
XM_006712513.2:c.190+209_190+211delinsCTG	XP_006712576.1:n.190+209_190+211delinsCTG
NM_002210.5:c.631+209_631+211delinsCTG MANE Select	NP_002201.2:n.631+209_631+211delinsCTG
NM_001145000.3:c.524-2499_524-2497delinsCTG	NP_001138472.2:n.524-2499_524-2497delinsCTG
NM_001144999.3:c.493+209_493+211delinsCTG	NP_001138471.2:n.493+209_493+211delinsCTG