Canonical Allele Identifier: CA1619341592

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859655T= , CM000668.2:g.31859655T=	GRCh38
NC_000006.11:g.31827432T= , CM000668.1:g.31827432T=	GRCh37
NC_000006.10:g.31935411T=	NCBI36
NG_008201.1:g.8278A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.*64A= MANE Select	ENSP00000364782.4:n.*64A=
ENST00000677054.1:n.2651A=
ENST00000677512.1:n.1589A=
ENST00000678869.1:n.1900A=
ENST00000375631.4:c.*64A=	ENSP00000364782.4:n.*64A=
ENST00000480384.1:n.1611A=
ENST00000491768.5:c.*422A=	ENSP00000433127.1:n.*422A=
ENST00000495807.1:n.2620A=
NM_000434.3:c.*64A=	NP_000425.1:n.*64A=
NM_000434.4:c.*64A= MANE Select	NP_000425.1:n.*64A=