Canonical Allele Identifier: CA363491837

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31828255C>A (hg19) ; chr6:g.31860478C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31860478C>A , CM000668.2:g.31860478C>A	GRCh38
NC_000006.11:g.31828255C>A , CM000668.1:g.31828255C>A	GRCh37
NC_000006.10:g.31936234C>A	NCBI36
NG_008201.1:g.7455G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.759G>T MANE Select	ENSP00000364782.4:p.Gln253His
ENST00000677054.1:n.2002G>T
ENST00000677512.1:n.867G>T
ENST00000678869.1:n.1433G>T
ENST00000375631.4:c.759G>T	ENSP00000364782.4:p.Gln253His
ENST00000480384.1:n.788G>T
ENST00000491768.5:c.759G>T	ENSP00000433127.1:p.Gln253His
ENST00000495807.1:n.1893G>T
NM_000434.3:c.759G>T	NP_000425.1:p.Gln253His
NM_000434.4:c.759G>T MANE Select	NP_000425.1:p.Gln253His