Canonical Allele Identifier: CA1619341599

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859680A= , CM000668.2:g.31859680A=	GRCh38
NC_000006.11:g.31827457A= , CM000668.1:g.31827457A=	GRCh37
NC_000006.10:g.31935436A=	NCBI36
NG_008201.1:g.8253T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.*39T= MANE Select	ENSP00000364782.4:n.*39T=
ENST00000677054.1:n.2626T=
ENST00000677512.1:n.1564T=
ENST00000678869.1:n.1875T=
ENST00000375631.4:c.*39T=	ENSP00000364782.4:n.*39T=
ENST00000480384.1:n.1586T=
ENST00000491768.5:c.*397T=	ENSP00000433127.1:n.*397T=
ENST00000495807.1:n.2595T=
NM_000434.3:c.*39T=	NP_000425.1:n.*39T=
NM_000434.4:c.*39T= MANE Select	NP_000425.1:n.*39T=