Canonical Allele Identifier: CA363491722
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31860471G>T , CM000668.2:g.31860471G>T GRCh38
NC_000006.11:g.31828248G>T , CM000668.1:g.31828248G>T GRCh37
NC_000006.10:g.31936227G>T NCBI36
NG_008201.1:g.7462C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.766C>A MANE Select ENSP00000364782.4:p.Gln256Lys
ENST00000677054.1:n.2009C>A
ENST00000677512.1:n.874C>A
ENST00000678869.1:n.1440C>A
ENST00000375631.4:c.766C>A ENSP00000364782.4:p.Gln256Lys
ENST00000480384.1:n.795C>A
ENST00000491768.5:c.766C>A ENSP00000433127.1:p.Gln256Lys
ENST00000495807.1:n.1900C>A
NM_000434.3:c.766C>A NP_000425.1:p.Gln256Lys
NM_000434.4:c.766C>A MANE Select NP_000425.1:p.Gln256Lys