Canonical Allele Identifier: CA2678053372
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31859640-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859640C>A , CM000668.2:g.31859640C>A GRCh38
NC_000006.11:g.31827417C>A , CM000668.1:g.31827417C>A GRCh37
NC_000006.10:g.31935396C>A NCBI36
NG_008201.1:g.8293G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.*79G>T MANE Select ENSP00000364782.4:n.*79G>T
ENST00000677054.1:n.2666G>T
ENST00000677512.1:n.1604G>T
ENST00000678869.1:n.1915G>T
ENST00000375631.4:c.*79G>T ENSP00000364782.4:n.*79G>T
ENST00000480384.1:n.1626G>T
ENST00000491768.5:c.*437G>T ENSP00000433127.1:n.*437G>T
ENST00000495807.1:n.2635G>T
NM_000434.3:c.*79G>T NP_000425.1:n.*79G>T
NM_000434.4:c.*79G>T MANE Select NP_000425.1:n.*79G>T
Search 100 bp 5'
Search 100 bp 3'