Canonical Allele Identifier: CA1619341602
Gene: NEU1 HGNC NCBI

Linked Data

dbSNP Id: rs1762425623

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859685T>C , CM000668.2:g.31859685T>C GRCh38
NC_000006.11:g.31827462T>C , CM000668.1:g.31827462T>C GRCh37
NC_000006.10:g.31935441T>C NCBI36
NG_008201.1:g.8248A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.*34A>G MANE Select ENSP00000364782.4:n.*34A>G
ENST00000677054.1:n.2621A>G
ENST00000677512.1:n.1559A>G
ENST00000678869.1:n.1870A>G
ENST00000375631.4:c.*34A>G ENSP00000364782.4:n.*34A>G
ENST00000480384.1:n.1581A>G
ENST00000491768.5:c.*392A>G ENSP00000433127.1:n.*392A>G
ENST00000495807.1:n.2590A>G
NM_000434.3:c.*34A>G NP_000425.1:n.*34A>G
NM_000434.4:c.*34A>G MANE Select NP_000425.1:n.*34A>G