Canonical Allele Identifier: CA1619341591

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859652C= , CM000668.2:g.31859652C=	GRCh38
NC_000006.11:g.31827429C= , CM000668.1:g.31827429C=	GRCh37
NC_000006.10:g.31935408C=	NCBI36
NG_008201.1:g.8281G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.*67G= MANE Select	ENSP00000364782.4:n.*67G=
ENST00000677054.1:n.2654G=
ENST00000677512.1:n.1592G=
ENST00000678869.1:n.1903G=
ENST00000375631.4:c.*67G=	ENSP00000364782.4:n.*67G=
ENST00000480384.1:n.1614G=
ENST00000491768.5:c.*425G=	ENSP00000433127.1:n.*425G=
ENST00000495807.1:n.2623G=
NM_000434.3:c.*67G=	NP_000425.1:n.*67G=
NM_000434.4:c.*67G= MANE Select	NP_000425.1:n.*67G=