Canonical Allele Identifier: CA2678053380
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31859661-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859661C>T , CM000668.2:g.31859661C>T GRCh38
NC_000006.11:g.31827438C>T , CM000668.1:g.31827438C>T GRCh37
NC_000006.10:g.31935417C>T NCBI36
NG_008201.1:g.8272G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.*58G>A MANE Select ENSP00000364782.4:n.*58G>A
ENST00000677054.1:n.2645G>A
ENST00000677512.1:n.1583G>A
ENST00000678869.1:n.1894G>A
ENST00000375631.4:c.*58G>A ENSP00000364782.4:n.*58G>A
ENST00000480384.1:n.1605G>A
ENST00000491768.5:c.*416G>A ENSP00000433127.1:n.*416G>A
ENST00000495807.1:n.2614G>A
NM_000434.3:c.*58G>A NP_000425.1:n.*58G>A
NM_000434.4:c.*58G>A MANE Select NP_000425.1:n.*58G>A
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