Canonical Allele Identifier: CA363486353

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31827722C>T (hg19) ; chr6:g.31859945C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859945C>T , CM000668.2:g.31859945C>T	GRCh38
NC_000006.11:g.31827722C>T , CM000668.1:g.31827722C>T	GRCh37
NC_000006.10:g.31935701C>T	NCBI36
NG_008201.1:g.7988G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.1022G>A MANE Select	ENSP00000364782.4:p.Arg341Gln
ENST00000677054.1:n.2361G>A
ENST00000677512.1:n.1299G>A
ENST00000678869.1:n.1610G>A
ENST00000375631.4:c.1022G>A	ENSP00000364782.4:p.Arg341Gln
ENST00000480384.1:n.1321G>A
ENST00000491768.5:c.*132G>A	ENSP00000433127.1:n.*132G>A
ENST00000495807.1:n.2330G>A
NM_000434.3:c.1022G>A	NP_000425.1:p.Arg341Gln
NM_000434.4:c.1022G>A MANE Select	NP_000425.1:p.Arg341Gln