Canonical Allele Identifier: CA363491521
Gene: NEU1 HGNC NCBI

Linked Data

dbSNP Id: rs1762464463

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31860460A>T , CM000668.2:g.31860460A>T GRCh38
NC_000006.11:g.31828237A>T , CM000668.1:g.31828237A>T GRCh37
NC_000006.10:g.31936216A>T NCBI36
NG_008201.1:g.7473T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.777T>A MANE Select ENSP00000364782.4:p.Asp259Glu
ENST00000677054.1:n.2020T>A
ENST00000677512.1:n.885T>A
ENST00000678869.1:n.1451T>A
ENST00000375631.4:c.777T>A ENSP00000364782.4:p.Asp259Glu
ENST00000480384.1:n.806T>A
ENST00000491768.5:c.777T>A ENSP00000433127.1:p.Asp259Glu
ENST00000495807.1:n.1911T>A
NM_000434.3:c.777T>A NP_000425.1:p.Asp259Glu
NM_000434.4:c.777T>A MANE Select NP_000425.1:p.Asp259Glu