Canonical Allele Identifier: CA1619341596
Gene: NEU1 HGNC NCBI

Linked Data

dbSNP Id: rs1762425290
gnomAD v4: 6-31859666-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859666G>C , CM000668.2:g.31859666G>C GRCh38
NC_000006.11:g.31827443G>C , CM000668.1:g.31827443G>C GRCh37
NC_000006.10:g.31935422G>C NCBI36
NG_008201.1:g.8267C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.*53C>G MANE Select ENSP00000364782.4:n.*53C>G
ENST00000677054.1:n.2640C>G
ENST00000677512.1:n.1578C>G
ENST00000678869.1:n.1889C>G
ENST00000375631.4:c.*53C>G ENSP00000364782.4:n.*53C>G
ENST00000480384.1:n.1600C>G
ENST00000491768.5:c.*411C>G ENSP00000433127.1:n.*411C>G
ENST00000495807.1:n.2609C>G
NM_000434.3:c.*53C>G NP_000425.1:n.*53C>G
NM_000434.4:c.*53C>G MANE Select NP_000425.1:n.*53C>G