Canonical Allele Identifier: CA1619341941

Gene: NEU1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.759G= MANE Select	ENSP00000364782.4:p.Gln253=
ENST00000677054.1:n.2002G=
ENST00000677512.1:n.867G=
ENST00000678869.1:n.1433G=
ENST00000375631.4:c.759G=	ENSP00000364782.4:p.Gln253=
ENST00000480384.1:n.788G=
ENST00000491768.5:c.759G=	ENSP00000433127.1:p.Gln253=
ENST00000495807.1:n.1893G=
NM_000434.3:c.759G=	NP_000425.1:p.Gln253=
NM_000434.4:c.759G= MANE Select	NP_000425.1:p.Gln253=