Canonical Allele Identifier: CA1618747828
Gene: HLA-E HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30490201G= , CM000668.2:g.30490201G= GRCh38
NC_000006.11:g.30457978G= , CM000668.1:g.30457978G= GRCh37
NC_000006.10:g.30565957G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376630.5:c.335-39G= MANE Select ENSP00000365817.4:n.335-39G=
ENST00000376630.4:c.335-39G= ENSP00000365817.4:n.335-39G=
ENST00000484194.1:n.562G=
ENST00000493699.1:n.485-39G=
NM_005516.5:c.335-39G= NP_005507.3:n.335-39G=
XM_017010807.1:c.458-39G= XP_016866296.1:n.458-39G=
XM_017010808.1:c.458-39G= XP_016866297.1:n.458-39G=
XM_017010809.2:c.335-39G= XP_016866298.1:n.335-39G=
NM_005516.6:c.335-39G= MANE Select NP_005507.3:n.335-39G=
Search 100 bp 5'
Search 100 bp 3'