Canonical Allele Identifier: CA363491710
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31860471-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31860471G>C , CM000668.2:g.31860471G>C GRCh38
NC_000006.11:g.31828248G>C , CM000668.1:g.31828248G>C GRCh37
NC_000006.10:g.31936227G>C NCBI36
NG_008201.1:g.7462C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.766C>G MANE Select ENSP00000364782.4:p.Gln256Glu
ENST00000677054.1:n.2009C>G
ENST00000677512.1:n.874C>G
ENST00000678869.1:n.1440C>G
ENST00000375631.4:c.766C>G ENSP00000364782.4:p.Gln256Glu
ENST00000480384.1:n.795C>G
ENST00000491768.5:c.766C>G ENSP00000433127.1:p.Gln256Glu
ENST00000495807.1:n.1900C>G
NM_000434.3:c.766C>G NP_000425.1:p.Gln256Glu
NM_000434.4:c.766C>G MANE Select NP_000425.1:p.Gln256Glu