Canonical Allele Identifier: CA363495543
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31862019A>T , CM000668.2:g.31862019A>T GRCh38
NC_000006.11:g.31829796A>T , CM000668.1:g.31829796A>T GRCh37
NC_000006.10:g.31937775A>T NCBI36
NG_008201.1:g.5914T>A
NG_023058.1:g.22028T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.332T>A MANE Select ENSP00000364782.4:p.Leu111Gln
ENST00000677054.1:n.461T>A
ENST00000677512.1:n.440T>A
ENST00000678869.1:n.440T>A
ENST00000375631.4:c.332T>A ENSP00000364782.4:p.Leu111Gln
ENST00000480384.1:n.361T>A
ENST00000491768.5:c.332T>A ENSP00000433127.1:p.Leu111Gln
ENST00000495807.1:n.352T>A
NM_000434.3:c.332T>A NP_000425.1:p.Leu111Gln
NM_000434.4:c.332T>A MANE Select NP_000425.1:p.Leu111Gln