Canonical Allele Identifier: CA1618747816
Gene: HLA-E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30490188T= , CM000668.2:g.30490188T= GRCh38
NC_000006.11:g.30457965T= , CM000668.1:g.30457965T= GRCh37
NC_000006.10:g.30565944T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376630.5:c.335-52T= MANE Select ENSP00000365817.4:n.335-52T=
ENST00000376630.4:c.335-52T= ENSP00000365817.4:n.335-52T=
ENST00000484194.1:n.549T=
ENST00000493699.1:n.485-52T=
NM_005516.5:c.335-52T= NP_005507.3:n.335-52T=
XM_017010807.1:c.458-52T= XP_016866296.1:n.458-52T=
XM_017010808.1:c.458-52T= XP_016866297.1:n.458-52T=
XM_017010809.2:c.335-52T= XP_016866298.1:n.335-52T=
NM_005516.6:c.335-52T= MANE Select NP_005507.3:n.335-52T=