Canonical Allele Identifier: CA363484715
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859748C>G , CM000668.2:g.31859748C>G GRCh38
NC_000006.11:g.31827525C>G , CM000668.1:g.31827525C>G GRCh37
NC_000006.10:g.31935504C>G NCBI36
NG_008201.1:g.8185G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.1219G>C MANE Select ENSP00000364782.4:p.Ala407Pro
ENST00000677054.1:n.2558G>C
ENST00000677512.1:n.1496G>C
ENST00000678869.1:n.1807G>C
ENST00000375631.4:c.1219G>C ENSP00000364782.4:p.Ala407Pro
ENST00000480384.1:n.1518G>C
ENST00000491768.5:c.*329G>C ENSP00000433127.1:n.*329G>C
ENST00000495807.1:n.2527G>C
NM_000434.3:c.1219G>C NP_000425.1:p.Ala407Pro
NM_000434.4:c.1219G>C MANE Select NP_000425.1:p.Ala407Pro