Canonical Allele Identifier: CA1619342298

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861398A= , CM000668.2:g.31861398A=	GRCh38
NC_000006.11:g.31829175A= , CM000668.1:g.31829175A=	GRCh37
NC_000006.10:g.31937154A=	NCBI36
NG_008201.1:g.6535T=
NG_023058.1:g.22649T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.405T= MANE Select	ENSP00000364782.4:p.Asp135=
ENST00000677054.1:n.1082T=
ENST00000677512.1:n.513T=
ENST00000678869.1:n.513T=
ENST00000375631.4:c.405T=	ENSP00000364782.4:p.Asp135=
ENST00000480384.1:n.434T=
ENST00000491768.5:c.405T=	ENSP00000433127.1:p.Asp135=
ENST00000495807.1:n.973T=
NM_000434.3:c.405T=	NP_000425.1:p.Asp135=
NM_000434.4:c.405T= MANE Select	NP_000425.1:p.Asp135=