Canonical Allele Identifier: CA363484692
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859745T>A , CM000668.2:g.31859745T>A GRCh38
NC_000006.11:g.31827522T>A , CM000668.1:g.31827522T>A GRCh37
NC_000006.10:g.31935501T>A NCBI36
NG_008201.1:g.8188A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.1222A>T MANE Select ENSP00000364782.4:p.Lys408Ter
ENST00000677054.1:n.2561A>T
ENST00000677512.1:n.1499A>T
ENST00000678869.1:n.1810A>T
ENST00000375631.4:c.1222A>T ENSP00000364782.4:p.Lys408Ter
ENST00000480384.1:n.1521A>T
ENST00000491768.5:c.*332A>T ENSP00000433127.1:n.*332A>T
ENST00000495807.1:n.2530A>T
NM_000434.3:c.1222A>T NP_000425.1:p.Lys408Ter
NM_000434.4:c.1222A>T MANE Select NP_000425.1:p.Lys408Ter