Canonical Allele Identifier: CA363495146
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861433T>C , CM000668.2:g.31861433T>C GRCh38
NC_000006.11:g.31829210T>C , CM000668.1:g.31829210T>C GRCh37
NC_000006.10:g.31937189T>C NCBI36
NG_008201.1:g.6500A>G
NG_023058.1:g.22614A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.370A>G MANE Select ENSP00000364782.4:p.Thr124Ala
ENST00000677054.1:n.1047A>G
ENST00000677512.1:n.478A>G
ENST00000678869.1:n.478A>G
ENST00000375631.4:c.370A>G ENSP00000364782.4:p.Thr124Ala
ENST00000480384.1:n.399A>G
ENST00000491768.5:c.370A>G ENSP00000433127.1:p.Thr124Ala
ENST00000495807.1:n.938A>G
NM_000434.3:c.370A>G NP_000425.1:p.Thr124Ala
NM_000434.4:c.370A>G MANE Select NP_000425.1:p.Thr124Ala