Canonical Allele Identifier: CA1619342272

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861317G= , CM000668.2:g.31861317G=	GRCh38
NC_000006.11:g.31829094G= , CM000668.1:g.31829094G=	GRCh37
NC_000006.10:g.31937073G=	NCBI36
NG_008201.1:g.6616C=
NG_023058.1:g.22730C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.486C= MANE Select	ENSP00000364782.4:p.Ala162=
ENST00000677054.1:n.1163C=
ENST00000677512.1:n.594C=
ENST00000678869.1:n.594C=
ENST00000375631.4:c.486C=	ENSP00000364782.4:p.Ala162=
ENST00000480384.1:n.515C=
ENST00000491768.5:c.486C=	ENSP00000433127.1:p.Ala162=
ENST00000495807.1:n.1054C=
NM_000434.3:c.486C=	NP_000425.1:p.Ala162=
NM_000434.4:c.486C= MANE Select	NP_000425.1:p.Ala162=