Canonical Allele Identifier: CA136925150

Gene: NEU1

Linked Data

• dbSNP Id: rs923866884
• gnomAD v3: 6-31859637-C-T
• gnomAD v4: 6-31859637-C-T
• MyVariant Identifiers: chr6:g.31827414C>T (hg19) ; chr6:g.31859637C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859637C>T , CM000668.2:g.31859637C>T	GRCh38
NC_000006.11:g.31827414C>T , CM000668.1:g.31827414C>T	GRCh37
NC_000006.10:g.31935393C>T	NCBI36
NG_008201.1:g.8296G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.*82G>A MANE Select	ENSP00000364782.4:n.*82G>A
ENST00000677054.1:n.2669G>A
ENST00000677512.1:n.1607G>A
ENST00000678869.1:n.1918G>A
ENST00000375631.4:c.*82G>A	ENSP00000364782.4:n.*82G>A
ENST00000480384.1:n.1629G>A
ENST00000491768.5:c.*440G>A	ENSP00000433127.1:n.*440G>A
ENST00000495807.1:n.2638G>A
NM_000434.3:c.*82G>A	NP_000425.1:n.*82G>A
NM_000434.4:c.*82G>A MANE Select	NP_000425.1:n.*82G>A