Canonical Allele Identifier: CA1619341629

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859752G= , CM000668.2:g.31859752G=	GRCh38
NC_000006.11:g.31827529G= , CM000668.1:g.31827529G=	GRCh37
NC_000006.10:g.31935508G=	NCBI36
NG_008201.1:g.8181C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.1215C= MANE Select	ENSP00000364782.4:p.Ser405=
ENST00000677054.1:n.2554C=
ENST00000677512.1:n.1492C=
ENST00000678869.1:n.1803C=
ENST00000375631.4:c.1215C=	ENSP00000364782.4:p.Ser405=
ENST00000480384.1:n.1514C=
ENST00000491768.5:c.*325C=	ENSP00000433127.1:n.*325C=
ENST00000495807.1:n.2523C=
NM_000434.3:c.1215C=	NP_000425.1:p.Ser405=
NM_000434.4:c.1215C= MANE Select	NP_000425.1:p.Ser405=