Canonical Allele Identifier: CA363491606
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31860467T>A , CM000668.2:g.31860467T>A GRCh38
NC_000006.11:g.31828244T>A , CM000668.1:g.31828244T>A GRCh37
NC_000006.10:g.31936223T>A NCBI36
NG_008201.1:g.7466A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.770A>T MANE Select ENSP00000364782.4:p.Glu257Val
ENST00000677054.1:n.2013A>T
ENST00000677512.1:n.878A>T
ENST00000678869.1:n.1444A>T
ENST00000375631.4:c.770A>T ENSP00000364782.4:p.Glu257Val
ENST00000480384.1:n.799A>T
ENST00000491768.5:c.770A>T ENSP00000433127.1:p.Glu257Val
ENST00000495807.1:n.1904A>T
NM_000434.3:c.770A>T NP_000425.1:p.Glu257Val
NM_000434.4:c.770A>T MANE Select NP_000425.1:p.Glu257Val