Canonical Allele Identifier: CA1619341706

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859938G= , CM000668.2:g.31859938G=	GRCh38
NC_000006.11:g.31827715G= , CM000668.1:g.31827715G=	GRCh37
NC_000006.10:g.31935694G=	NCBI36
NG_008201.1:g.7995C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.1029C= MANE Select	ENSP00000364782.4:p.Asn343=
ENST00000677054.1:n.2368C=
ENST00000677512.1:n.1306C=
ENST00000678869.1:n.1617C=
ENST00000375631.4:c.1029C=	ENSP00000364782.4:p.Asn343=
ENST00000480384.1:n.1328C=
ENST00000491768.5:c.*139C=	ENSP00000433127.1:n.*139C=
ENST00000495807.1:n.2337C=
NM_000434.3:c.1029C=	NP_000425.1:p.Asn343=
NM_000434.4:c.1029C= MANE Select	NP_000425.1:p.Asn343=