Canonical Allele Identifier: CA2678053390
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31859675-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859675G>T , CM000668.2:g.31859675G>T GRCh38
NC_000006.11:g.31827452G>T , CM000668.1:g.31827452G>T GRCh37
NC_000006.10:g.31935431G>T NCBI36
NG_008201.1:g.8258C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.*44C>A MANE Select ENSP00000364782.4:n.*44C>A
ENST00000677054.1:n.2631C>A
ENST00000677512.1:n.1569C>A
ENST00000678869.1:n.1880C>A
ENST00000375631.4:c.*44C>A ENSP00000364782.4:n.*44C>A
ENST00000480384.1:n.1591C>A
ENST00000491768.5:c.*402C>A ENSP00000433127.1:n.*402C>A
ENST00000495807.1:n.2600C>A
NM_000434.3:c.*44C>A NP_000425.1:n.*44C>A
NM_000434.4:c.*44C>A MANE Select NP_000425.1:n.*44C>A
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