Canonical Allele Identifier: CA1619342292

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861379C= , CM000668.2:g.31861379C=	GRCh38
NC_000006.11:g.31829156C= , CM000668.1:g.31829156C=	GRCh37
NC_000006.10:g.31937135C=	NCBI36
NG_008201.1:g.6554G=
NG_023058.1:g.22668G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.424G= MANE Select	ENSP00000364782.4:p.Val142=
ENST00000677054.1:n.1101G=
ENST00000677512.1:n.532G=
ENST00000678869.1:n.532G=
ENST00000375631.4:c.424G=	ENSP00000364782.4:p.Val142=
ENST00000480384.1:n.453G=
ENST00000491768.5:c.424G=	ENSP00000433127.1:p.Val142=
ENST00000495807.1:n.992G=
NM_000434.3:c.424G=	NP_000425.1:p.Val142=
NM_000434.4:c.424G= MANE Select	NP_000425.1:p.Val142=