Canonical Allele Identifier: CA1619341601

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859685T= , CM000668.2:g.31859685T=	GRCh38
NC_000006.11:g.31827462T= , CM000668.1:g.31827462T=	GRCh37
NC_000006.10:g.31935441T=	NCBI36
NG_008201.1:g.8248A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.*34A= MANE Select	ENSP00000364782.4:n.*34A=
ENST00000677054.1:n.2621A=
ENST00000677512.1:n.1559A=
ENST00000678869.1:n.1870A=
ENST00000375631.4:c.*34A=	ENSP00000364782.4:n.*34A=
ENST00000480384.1:n.1581A=
ENST00000491768.5:c.*392A=	ENSP00000433127.1:n.*392A=
ENST00000495807.1:n.2590A=
NM_000434.3:c.*34A=	NP_000425.1:n.*34A=
NM_000434.4:c.*34A= MANE Select	NP_000425.1:n.*34A=