Canonical Allele Identifier: CA1619341760

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31860055T= , CM000668.2:g.31860055T=	GRCh38
NC_000006.11:g.31827832T= , CM000668.1:g.31827832T=	GRCh37
NC_000006.10:g.31935811T=	NCBI36
NG_008201.1:g.7878A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.1008A= MANE Select	ENSP00000364782.4:p.Ala336=
ENST00000677054.1:n.2251A=
ENST00000677512.1:n.1290A=
ENST00000678869.1:n.1596A=
ENST00000375631.4:c.1008A=	ENSP00000364782.4:p.Ala336=
ENST00000480384.1:n.1211A=
ENST00000491768.5:c.*118A=	ENSP00000433127.1:n.*118A=
ENST00000495807.1:n.2316A=
NM_000434.3:c.1008A=	NP_000425.1:p.Ala336=
NM_000434.4:c.1008A= MANE Select	NP_000425.1:p.Ala336=