Canonical Allele Identifier: CA363494491
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861325G>A , CM000668.2:g.31861325G>A GRCh38
NC_000006.11:g.31829102G>A , CM000668.1:g.31829102G>A GRCh37
NC_000006.10:g.31937081G>A NCBI36
NG_008201.1:g.6608C>T
NG_023058.1:g.22722C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.478C>T MANE Select ENSP00000364782.4:p.His160Tyr
ENST00000677054.1:n.1155C>T
ENST00000677512.1:n.586C>T
ENST00000678869.1:n.586C>T
ENST00000375631.4:c.478C>T ENSP00000364782.4:p.His160Tyr
ENST00000480384.1:n.507C>T
ENST00000491768.5:c.478C>T ENSP00000433127.1:p.His160Tyr
ENST00000495807.1:n.1046C>T
NM_000434.3:c.478C>T NP_000425.1:p.His160Tyr
NM_000434.4:c.478C>T MANE Select NP_000425.1:p.His160Tyr