Canonical Allele Identifier: CA2677798158
Gene: HLA-A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29945691_29945692insC , CM000668.2:g.29945691_29945692insC GRCh38
NC_000006.11:g.29913468_29913469insC , CM000668.1:g.29913468_29913469insC GRCh37
NC_000006.10:g.30021447_30021448insC NCBI36
NG_029217.2:g.8227_8228insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000638375.2:c.1217_1218insC ENSP00000492789.2:n.1217_1218insC
ENST00000706892.1:n.3043_3044insC
ENST00000706893.1:c.*318_*319insC ENSP00000516609.1:n.*318_*319insC
ENST00000706894.1:c.*318_*319insC ENSP00000516610.1:n.*318_*319insC
ENST00000706895.1:n.2323_2324insC
ENST00000706896.1:n.2630_2631insC
ENST00000706897.1:n.2052_2053insC
ENST00000706898.1:c.*236_*237insC ENSP00000516611.1:n.*236_*237insC
ENST00000706899.1:n.2188_2189insC
ENST00000706900.1:c.*236_*237insC ENSP00000516617.1:n.*236_*237insC
ENST00000706901.1:c.*236_*237insC ENSP00000516612.1:n.*236_*237insC
ENST00000706902.1:c.1093+410_1093+411insC ENSP00000516613.1:n.1093+410_1093+411insC
ENST00000706903.1:c.*124+112_*124+113insC ENSP00000516614.1:n.*124+112_*124+113insC
ENST00000706904.1:c.1093+410_1093+411insC ENSP00000516615.1:n.1093+410_1093+411insC
ENST00000706905.1:c.*236_*237insC ENSP00000516616.1:n.*236_*237insC
ENST00000376809.10:c.*236_*237insC MANE Select ENSP00000366005.5:n.*236_*237insC
ENST00000376802.2:c.*236_*237insC ENSP00000365998.2:n.*236_*237insC
ENST00000376806.9:c.*236_*237insC ENSP00000366002.5:n.*236_*237insC
ENST00000376809.9:c.*236_*237insC ENSP00000366005.5:n.*236_*237insC
ENST00000396634.5:c.*236_*237insC ENSP00000379873.1:n.*236_*237insC
ENST00000495183.5:n.1573_1574insC
ENST00000496081.5:n.1593_1594insC
NM_002116.7:c.*236_*237insC NP_002107.3:n.*236_*237insC
NM_002116.8:c.*236_*237insC MANE Select NP_002107.3:n.*236_*237insC