Canonical Allele Identifier: CA1619341597

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859666G= , CM000668.2:g.31859666G=	GRCh38
NC_000006.11:g.31827443G= , CM000668.1:g.31827443G=	GRCh37
NC_000006.10:g.31935422G=	NCBI36
NG_008201.1:g.8267C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.*53C= MANE Select	ENSP00000364782.4:n.*53C=
ENST00000677054.1:n.2640C=
ENST00000677512.1:n.1578C=
ENST00000678869.1:n.1889C=
ENST00000375631.4:c.*53C=	ENSP00000364782.4:n.*53C=
ENST00000480384.1:n.1600C=
ENST00000491768.5:c.*411C=	ENSP00000433127.1:n.*411C=
ENST00000495807.1:n.2609C=
NM_000434.3:c.*53C=	NP_000425.1:n.*53C=
NM_000434.4:c.*53C= MANE Select	NP_000425.1:n.*53C=