Canonical Allele Identifier: CA363495264
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861450C>G , CM000668.2:g.31861450C>G GRCh38
NC_000006.11:g.31829227C>G , CM000668.1:g.31829227C>G GRCh37
NC_000006.10:g.31937206C>G NCBI36
NG_008201.1:g.6483G>C
NG_023058.1:g.22597G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.353G>C MANE Select ENSP00000364782.4:p.Gly118Ala
ENST00000677054.1:n.1030G>C
ENST00000677512.1:n.461G>C
ENST00000678869.1:n.461G>C
ENST00000375631.4:c.353G>C ENSP00000364782.4:p.Gly118Ala
ENST00000480384.1:n.382G>C
ENST00000491768.5:c.353G>C ENSP00000433127.1:p.Gly118Ala
ENST00000495807.1:n.921G>C
NM_000434.3:c.353G>C NP_000425.1:p.Gly118Ala
NM_000434.4:c.353G>C MANE Select NP_000425.1:p.Gly118Ala