Canonical Allele Identifier: CA2678054010

Gene: NEU1

Linked Data

• gnomAD v4: 6-31861636-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861636T>C , CM000668.2:g.31861636T>C	GRCh38
NC_000006.11:g.31829413T>C , CM000668.1:g.31829413T>C	GRCh37
NC_000006.10:g.31937392T>C	NCBI36
NG_008201.1:g.6297A>G
NG_023058.1:g.22411A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-186A>G MANE Select	ENSP00000364782.4:n.353-186A>G
ENST00000677054.1:n.844A>G
ENST00000677512.1:n.461-186A>G
ENST00000678869.1:n.461-186A>G
ENST00000375631.4:c.353-186A>G	ENSP00000364782.4:n.353-186A>G
ENST00000480384.1:n.382-186A>G
ENST00000491768.5:c.353-186A>G	ENSP00000433127.1:n.353-186A>G
ENST00000495807.1:n.735A>G
NM_000434.3:c.353-186A>G	NP_000425.1:n.353-186A>G
NM_000434.4:c.353-186A>G MANE Select	NP_000425.1:n.353-186A>G