Canonical Allele Identifier: CA363491622
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31860468C>G , CM000668.2:g.31860468C>G GRCh38
NC_000006.11:g.31828245C>G , CM000668.1:g.31828245C>G GRCh37
NC_000006.10:g.31936224C>G NCBI36
NG_008201.1:g.7465G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.769G>C MANE Select ENSP00000364782.4:p.Glu257Gln
ENST00000677054.1:n.2012G>C
ENST00000677512.1:n.877G>C
ENST00000678869.1:n.1443G>C
ENST00000375631.4:c.769G>C ENSP00000364782.4:p.Glu257Gln
ENST00000480384.1:n.798G>C
ENST00000491768.5:c.769G>C ENSP00000433127.1:p.Glu257Gln
ENST00000495807.1:n.1903G>C
NM_000434.3:c.769G>C NP_000425.1:p.Glu257Gln
NM_000434.4:c.769G>C MANE Select NP_000425.1:p.Glu257Gln