Canonical Allele Identifier: CA2678053956

Gene: NEU1

Linked Data

• gnomAD v4: 6-31861569-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861569G>T , CM000668.2:g.31861569G>T	GRCh38
NC_000006.11:g.31829346G>T , CM000668.1:g.31829346G>T	GRCh37
NC_000006.10:g.31937325G>T	NCBI36
NG_008201.1:g.6364C>A
NG_023058.1:g.22478C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-119C>A MANE Select	ENSP00000364782.4:n.353-119C>A
ENST00000677054.1:n.911C>A
ENST00000677512.1:n.461-119C>A
ENST00000678869.1:n.461-119C>A
ENST00000375631.4:c.353-119C>A	ENSP00000364782.4:n.353-119C>A
ENST00000480384.1:n.382-119C>A
ENST00000491768.5:c.353-119C>A	ENSP00000433127.1:n.353-119C>A
ENST00000495807.1:n.802C>A
NM_000434.3:c.353-119C>A	NP_000425.1:n.353-119C>A
NM_000434.4:c.353-119C>A MANE Select	NP_000425.1:n.353-119C>A