Canonical Allele Identifier: CA1899184054

Gene: JCAD

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30027152G= , CM000672.2:g.30027152G=	GRCh38
NC_000010.10:g.30316081G= , CM000672.1:g.30316081G=	GRCh37
NC_000010.9:g.30356087G=	NCBI36
NG_053080.1:g.93343C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375377.2:c.2996C= MANE Select	ENSP00000364526.1:p.Pro999=
ENST00000375377.1:c.2996C=	ENSP00000364526.1:p.Pro999=
NM_020848.2:c.2996C=	NP_065899.1:p.Pro999=
XM_011519608.1:c.2996C=	XP_011517910.1:p.Pro999=
XM_011519609.1:c.2582C=	XP_011517911.1:p.Pro861=
XM_011519610.1:c.2582C=	XP_011517912.1:p.Pro861=
NM_001350001.1:c.2582C=	NP_001336930.1:p.Pro861=
NM_001350021.1:c.2582C=	NP_001336950.1:p.Pro861=
NM_001350022.1:c.2996C=	NP_001336951.1:p.Pro999=
NM_020848.3:c.2996C=	NP_065899.1:p.Pro999=
NM_020848.4:c.2996C= MANE Select	NP_065899.1:p.Pro999=
NM_001350001.2:c.2582C=	NP_001336930.1:p.Pro861=
NM_001350021.2:c.2582C=	NP_001336950.1:p.Pro861=
NM_001350022.2:c.2996C=	NP_001336951.1:p.Pro999=