Canonical Allele Identifier: CA1619342320

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861440C= , CM000668.2:g.31861440C=	GRCh38
NC_000006.11:g.31829217C= , CM000668.1:g.31829217C=	GRCh37
NC_000006.10:g.31937196C=	NCBI36
NG_008201.1:g.6493G=
NG_023058.1:g.22607G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.363G= MANE Select	ENSP00000364782.4:p.Trp121=
ENST00000677054.1:n.1040G=
ENST00000677512.1:n.471G=
ENST00000678869.1:n.471G=
ENST00000375631.4:c.363G=	ENSP00000364782.4:p.Trp121=
ENST00000480384.1:n.392G=
ENST00000491768.5:c.363G=	ENSP00000433127.1:p.Trp121=
ENST00000495807.1:n.931G=
NM_000434.3:c.363G=	NP_000425.1:p.Trp121=
NM_000434.4:c.363G= MANE Select	NP_000425.1:p.Trp121=