Canonical Allele Identifier: CA2678054004

Gene: NEU1

Linked Data

• gnomAD v4: 6-31861629-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861629T>A , CM000668.2:g.31861629T>A	GRCh38
NC_000006.11:g.31829406T>A , CM000668.1:g.31829406T>A	GRCh37
NC_000006.10:g.31937385T>A	NCBI36
NG_008201.1:g.6304A>T
NG_023058.1:g.22418A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-179A>T MANE Select	ENSP00000364782.4:n.353-179A>T
ENST00000677054.1:n.851A>T
ENST00000677512.1:n.461-179A>T
ENST00000678869.1:n.461-179A>T
ENST00000375631.4:c.353-179A>T	ENSP00000364782.4:n.353-179A>T
ENST00000480384.1:n.382-179A>T
ENST00000491768.5:c.353-179A>T	ENSP00000433127.1:n.353-179A>T
ENST00000495807.1:n.742A>T
NM_000434.3:c.353-179A>T	NP_000425.1:n.353-179A>T
NM_000434.4:c.353-179A>T MANE Select	NP_000425.1:n.353-179A>T