Canonical Allele Identifier: CA1618747819
Gene: HLA-E HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30490191C= , CM000668.2:g.30490191C= GRCh38
NC_000006.11:g.30457968C= , CM000668.1:g.30457968C= GRCh37
NC_000006.10:g.30565947C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376630.5:c.335-49C= MANE Select ENSP00000365817.4:n.335-49C=
ENST00000376630.4:c.335-49C= ENSP00000365817.4:n.335-49C=
ENST00000484194.1:n.552C=
ENST00000493699.1:n.485-49C=
NM_005516.5:c.335-49C= NP_005507.3:n.335-49C=
XM_017010807.1:c.458-49C= XP_016866296.1:n.458-49C=
XM_017010808.1:c.458-49C= XP_016866297.1:n.458-49C=
XM_017010809.2:c.335-49C= XP_016866298.1:n.335-49C=
NM_005516.6:c.335-49C= MANE Select NP_005507.3:n.335-49C=