Canonical Allele Identifier: CA363491618
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.770A>C MANE Select ENSP00000364782.4:p.Glu257Ala
ENST00000677054.1:n.2013A>C
ENST00000677512.1:n.878A>C
ENST00000678869.1:n.1444A>C
ENST00000375631.4:c.770A>C ENSP00000364782.4:p.Glu257Ala
ENST00000480384.1:n.799A>C
ENST00000491768.5:c.770A>C ENSP00000433127.1:p.Glu257Ala
ENST00000495807.1:n.1904A>C
NM_000434.3:c.770A>C NP_000425.1:p.Glu257Ala
NM_000434.4:c.770A>C MANE Select NP_000425.1:p.Glu257Ala