Canonical Allele Identifier: CA2678053387
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31859671-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859671T>C , CM000668.2:g.31859671T>C GRCh38
NC_000006.11:g.31827448T>C , CM000668.1:g.31827448T>C GRCh37
NC_000006.10:g.31935427T>C NCBI36
NG_008201.1:g.8262A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.*48A>G MANE Select ENSP00000364782.4:n.*48A>G
ENST00000677054.1:n.2635A>G
ENST00000677512.1:n.1573A>G
ENST00000678869.1:n.1884A>G
ENST00000375631.4:c.*48A>G ENSP00000364782.4:n.*48A>G
ENST00000480384.1:n.1595A>G
ENST00000491768.5:c.*406A>G ENSP00000433127.1:n.*406A>G
ENST00000495807.1:n.2604A>G
NM_000434.3:c.*48A>G NP_000425.1:n.*48A>G
NM_000434.4:c.*48A>G MANE Select NP_000425.1:n.*48A>G