Canonical Allele Identifier: CA1619342306

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861416A= , CM000668.2:g.31861416A=	GRCh38
NC_000006.11:g.31829193A= , CM000668.1:g.31829193A=	GRCh37
NC_000006.10:g.31937172A=	NCBI36
NG_008201.1:g.6517T=
NG_023058.1:g.22631T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.387T= MANE Select	ENSP00000364782.4:p.Asn129=
ENST00000677054.1:n.1064T=
ENST00000677512.1:n.495T=
ENST00000678869.1:n.495T=
ENST00000375631.4:c.387T=	ENSP00000364782.4:p.Asn129=
ENST00000480384.1:n.416T=
ENST00000491768.5:c.387T=	ENSP00000433127.1:p.Asn129=
ENST00000495807.1:n.955T=
NM_000434.3:c.387T=	NP_000425.1:p.Asn129=
NM_000434.4:c.387T= MANE Select	NP_000425.1:p.Asn129=