Canonical Allele Identifier: CA2678053388
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31859672-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859672G>A , CM000668.2:g.31859672G>A GRCh38
NC_000006.11:g.31827449G>A , CM000668.1:g.31827449G>A GRCh37
NC_000006.10:g.31935428G>A NCBI36
NG_008201.1:g.8261C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.*47C>T MANE Select ENSP00000364782.4:n.*47C>T
ENST00000677054.1:n.2634C>T
ENST00000677512.1:n.1572C>T
ENST00000678869.1:n.1883C>T
ENST00000375631.4:c.*47C>T ENSP00000364782.4:n.*47C>T
ENST00000480384.1:n.1594C>T
ENST00000491768.5:c.*405C>T ENSP00000433127.1:n.*405C>T
ENST00000495807.1:n.2603C>T
NM_000434.3:c.*47C>T NP_000425.1:n.*47C>T
NM_000434.4:c.*47C>T MANE Select NP_000425.1:n.*47C>T