Canonical Allele Identifier: CA2677847742
Gene: HLA-E HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30490206_30490236del , CM000668.2:g.30490206_30490236del GRCh38
NC_000006.11:g.30457983_30458013del , CM000668.1:g.30457983_30458013del GRCh37
NC_000006.10:g.30565962_30565992del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376630.5:c.335-34_335-4del MANE Select ENSP00000365817.4:n.335-34_335-4del
ENST00000376630.4:c.335-34_335-4del ENSP00000365817.4:n.335-34_335-4del
ENST00000484194.1:n.567_597del
ENST00000493699.1:n.485-34_485-4del
NM_005516.5:c.335-34_335-4del NP_005507.3:n.335-34_335-4del
XM_017010807.1:c.458-34_458-4del XP_016866296.1:n.458-34_458-4del
XM_017010808.1:c.458-34_458-4del XP_016866297.1:n.458-34_458-4del
XM_017010809.2:c.335-34_335-4del XP_016866298.1:n.335-34_335-4del
NM_005516.6:c.335-34_335-4del MANE Select NP_005507.3:n.335-34_335-4del