Canonical Allele Identifier: CA2662275484
Gene: ITGAV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.186633512_186633513insA , CM000664.2:g.186633512_186633513insA GRCh38
NC_000002.11:g.187498239_187498240insA , CM000664.1:g.187498239_187498240insA GRCh37
NC_000002.10:g.187206484_187206485insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000696906.1:c.631+138_631+139insA ENSP00000512967.1:n.631+138_631+139insA
ENST00000696907.1:c.454+138_454+139insA ENSP00000512968.1:n.454+138_454+139insA
ENST00000696908.1:c.*41+138_*41+139insA ENSP00000512969.1:n.*41+138_*41+139insA
ENST00000696909.1:c.454+138_454+139insA ENSP00000512970.1:n.454+138_454+139insA
ENST00000696910.1:c.631+138_631+139insA ENSP00000512971.1:n.631+138_631+139insA
ENST00000696911.1:c.631+138_631+139insA ENSP00000512972.1:n.631+138_631+139insA
ENST00000696912.1:c.631+138_631+139insA ENSP00000512973.1:n.631+138_631+139insA
ENST00000696913.1:c.631+138_631+139insA ENSP00000512974.1:n.631+138_631+139insA
ENST00000696914.1:c.*183+138_*183+139insA ENSP00000512975.1:n.*183+138_*183+139insA
ENST00000696917.1:n.1140+138_1140+139insA
ENST00000696936.1:n.901+138_901+139insA
ENST00000696937.1:c.631+138_631+139insA ENSP00000512982.1:n.631+138_631+139insA
ENST00000261023.8:c.631+138_631+139insA MANE Select ENSP00000261023.3:n.631+138_631+139insA
ENST00000261023.7:c.631+138_631+139insA ENSP00000261023.3:n.631+138_631+139insA
ENST00000374907.7:c.524-2570_524-2569insA ENSP00000364042.3:n.524-2570_524-2569insA
ENST00000433736.6:c.493+138_493+139insA ENSP00000404291.2:n.493+138_493+139insA
NM_001144999.2:c.493+138_493+139insA NP_001138471.1:n.493+138_493+139insA
NM_001145000.2:c.524-2570_524-2569insA NP_001138472.1:n.524-2570_524-2569insA
NM_002210.4:c.631+138_631+139insA NP_002201.1:n.631+138_631+139insA
XM_006712513.2:c.190+138_190+139insA XP_006712576.1:n.190+138_190+139insA
NM_002210.5:c.631+138_631+139insA MANE Select NP_002201.2:n.631+138_631+139insA
NM_001145000.3:c.524-2570_524-2569insA NP_001138472.2:n.524-2570_524-2569insA
NM_001144999.3:c.493+138_493+139insA NP_001138471.2:n.493+138_493+139insA