Canonical Allele Identifier: CA2678054019

Gene: NEU1

Linked Data

• gnomAD v4: 6-31861646-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861652dup , CM000668.2:g.31861652dup	GRCh38
NC_000006.11:g.31829429dup , CM000668.1:g.31829429dup	GRCh37
NC_000006.10:g.31937408dup	NCBI36
NG_008201.1:g.6286dup
NG_023058.1:g.22400dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-197dup MANE Select	ENSP00000364782.4:n.353-197dup
ENST00000677054.1:n.833dup
ENST00000677512.1:n.461-197dup
ENST00000678869.1:n.461-197dup
ENST00000375631.4:c.353-197dup	ENSP00000364782.4:n.353-197dup
ENST00000480384.1:n.382-197dup
ENST00000491768.5:c.353-197dup	ENSP00000433127.1:n.353-197dup
ENST00000495807.1:n.724dup
NM_000434.3:c.353-197dup	NP_000425.1:n.353-197dup
NM_000434.4:c.353-197dup MANE Select	NP_000425.1:n.353-197dup