Canonical Allele Identifier: CA1619341585

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859638G= , CM000668.2:g.31859638G=	GRCh38
NC_000006.11:g.31827415G= , CM000668.1:g.31827415G=	GRCh37
NC_000006.10:g.31935394G=	NCBI36
NG_008201.1:g.8295C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.*81C= MANE Select	ENSP00000364782.4:n.*81C=
ENST00000677054.1:n.2668C=
ENST00000677512.1:n.1606C=
ENST00000678869.1:n.1917C=
ENST00000375631.4:c.*81C=	ENSP00000364782.4:n.*81C=
ENST00000480384.1:n.1628C=
ENST00000491768.5:c.*439C=	ENSP00000433127.1:n.*439C=
ENST00000495807.1:n.2637C=
NM_000434.3:c.*81C=	NP_000425.1:n.*81C=
NM_000434.4:c.*81C= MANE Select	NP_000425.1:n.*81C=