Canonical Allele Identifier: CA3111628157

Gene: UCHL1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.41256996A= , CM000666.2:g.41256996A=	GRCh38
NC_000004.11:g.41259013A= , CM000666.1:g.41259013A=	GRCh37
NC_000004.10:g.40953770A=	NCBI36
NG_012931.1:g.5116A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004181.5:c.20A= MANE Select	NP_004172.2:p.Glu7=
ENST00000284440.9:c.20A= MANE Select	ENSP00000284440.4:p.Glu7=
NM_004181.4:c.20A=	NP_004172.2:p.Glu7=
ENST00000284440.8:c.20A=	ENSP00000284440.4:p.Glu7=
ENST00000381760.8:n.89A=
ENST00000472501.5:n.51A=
ENST00000503431.5:c.20A=	ENSP00000422542.1:p.Glu7=
ENST00000504818.5:n.64A=
ENST00000505232.5:c.20A=	ENSP00000423348.1:p.Glu7=
ENST00000508768.5:c.20A=	ENSP00000426895.1:p.Glu7=
ENST00000512419.5:c.20A=	ENSP00000425714.1:p.Glu7=
ENST00000512788.1:c.20A=	ENSP00000423623.1:p.Glu7=
ENST00000514924.5:c.20A=	ENSP00000426634.1:p.Glu7=