Canonical Allele Identifier: CA2695206091
Gene: HLA-A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29943279_29943287delinsCTCCAGATG , CM000668.2:g.29943279_29943287delinsCTCCAGATG GRCh38
NC_000006.11:g.29911056_29911064delinsCTCCAGATG , CM000668.1:g.29911056_29911064delinsCTCCAGATG GRCh37
NC_000006.10:g.30019035_30019043delinsCTCCAGATG NCBI36
NG_029217.2:g.5814_5822delinsCTCCAGATG

Transcript Alleles

HGVS Amino-acid change
ENST00000638375.2:c.355_363delinsCTCCAGATG ENSP00000492789.2:p.Ile119_Ile121delinsLe...
ENST00000706892.1:n.631_639delinsCTCCAGATG
ENST00000706893.1:c.355_363delinsCTCCAGATG ENSP00000516609.1:p.Ile119_Ile121delinsLe...
ENST00000706894.1:c.355_363delinsCTCCAGATG ENSP00000516610.1:p.Ile119_Ile121delinsLe...
ENST00000706895.1:n.631_639delinsCTCCAGATG
ENST00000706896.1:n.631_639delinsCTCCAGATG
ENST00000706897.1:n.631_639delinsCTCCAGATG
ENST00000706898.1:c.355_363delinsCTCCAGATG ENSP00000516611.1:p.Ile119_Ile121delinsLe...
ENST00000706899.1:n.631_639delinsCTCCAGATG
ENST00000706900.1:c.271_279delinsCTCCAGATG ENSP00000516617.1:p.Ile91_Ile93delinsLeuG...
ENST00000706901.1:c.355_363delinsCTCCAGATG ENSP00000516612.1:p.Ile119_Ile121delinsLe...
ENST00000706902.1:c.355_363delinsCTCCAGATG ENSP00000516613.1:p.Ile119_Ile121delinsLe...
ENST00000706903.1:c.355_363delinsCTCCAGATG ENSP00000516614.1:p.Ile119_Ile121delinsLe...
ENST00000706904.1:c.355_363delinsCTCCAGATG ENSP00000516615.1:p.Ile119_Ile121delinsLe...
ENST00000706905.1:c.355_363delinsCTCCAGATG ENSP00000516616.1:p.Ile119_Ile121delinsLe...
ENST00000376809.10:c.355_363delinsCTCCAGATG MANE Select ENSP00000366005.5:p.Ile119_Ile121delinsLe...
ENST00000638375.1:c.355_363delinsCTCCAGATG ENSP00000492789.1:p.Ile119_Ile121delinsLe...
ENST00000376802.2:c.355_363delinsCTCCAGATG ENSP00000365998.2:p.Ile119_Ile121delinsLe...
ENST00000376806.9:c.355_363delinsCTCCAGATG ENSP00000366002.5:p.Ile119_Ile121delinsLe...
ENST00000376809.9:c.355_363delinsCTCCAGATG ENSP00000366005.5:p.Ile119_Ile121delinsLe...
ENST00000396634.5:c.355_363delinsCTCCAGATG ENSP00000379873.1:p.Ile119_Ile121delinsLe...
ENST00000461903.1:n.596_604delinsCTCCAGATG
ENST00000479320.5:n.596_604delinsCTCCAGATG
ENST00000495183.5:n.598_606delinsCTCCAGATG
ENST00000496081.5:n.178-6_180delinsCTCCAGATG
NM_002116.7:c.355_363delinsCTCCAGATG NP_002107.3:p.Ile119_Ile121delinsLeuGlnMe...
NM_002116.8:c.355_363delinsCTCCAGATG MANE Select NP_002107.3:p.Ile119_Ile121delinsLeuGlnMe...