Canonical Allele Identifier: CA1899184051

Gene: JCAD

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30027147C= , CM000672.2:g.30027147C=	GRCh38
NC_000010.10:g.30316076C= , CM000672.1:g.30316076C=	GRCh37
NC_000010.9:g.30356082C=	NCBI36
NG_053080.1:g.93348G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375377.2:c.3001G= MANE Select	ENSP00000364526.1:p.Glu1001=
ENST00000375377.1:c.3001G=	ENSP00000364526.1:p.Glu1001=
NM_020848.2:c.3001G=	NP_065899.1:p.Glu1001=
XM_011519608.1:c.3001G=	XP_011517910.1:p.Glu1001=
XM_011519609.1:c.2587G=	XP_011517911.1:p.Glu863=
XM_011519610.1:c.2587G=	XP_011517912.1:p.Glu863=
NM_001350001.1:c.2587G=	NP_001336930.1:p.Glu863=
NM_001350021.1:c.2587G=	NP_001336950.1:p.Glu863=
NM_001350022.1:c.3001G=	NP_001336951.1:p.Glu1001=
NM_020848.3:c.3001G=	NP_065899.1:p.Glu1001=
NM_020848.4:c.3001G= MANE Select	NP_065899.1:p.Glu1001=
NM_001350001.2:c.2587G=	NP_001336930.1:p.Glu863=
NM_001350021.2:c.2587G=	NP_001336950.1:p.Glu863=
NM_001350022.2:c.3001G=	NP_001336951.1:p.Glu1001=