Canonical Allele Identifier: CA2787127668

Gene: JCAD

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30034987A>T , CM000672.2:g.30034987A>T	GRCh38
NC_000010.10:g.30323916A>T , CM000672.1:g.30323916A>T	GRCh37
NC_000010.9:g.30363922A>T	NCBI36
NG_053080.1:g.85508T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375377.2:c.282-5121T>A MANE Select	ENSP00000364526.1:n.282-5121T>A
ENST00000375377.1:c.282-5121T>A	ENSP00000364526.1:n.282-5121T>A
NM_020848.2:c.282-5121T>A	NP_065899.1:n.282-5121T>A
XM_011519608.1:c.282-5121T>A	XP_011517910.1:n.282-5121T>A
XM_011519609.1:c.-133-5121T>A	XP_011517911.1:n.-133-5121T>A
XM_011519610.1:c.-133-5121T>A	XP_011517912.1:n.-133-5121T>A
NM_001350001.1:c.-133-5121T>A	NP_001336930.1:n.-133-5121T>A
NM_001350021.1:c.-133-5121T>A	NP_001336950.1:n.-133-5121T>A
NM_001350022.1:c.282-5121T>A	NP_001336951.1:n.282-5121T>A
NM_020848.3:c.282-5121T>A	NP_065899.1:n.282-5121T>A
NM_020848.4:c.282-5121T>A MANE Select	NP_065899.1:n.282-5121T>A
NM_001350001.2:c.-133-5121T>A	NP_001336930.1:n.-133-5121T>A
NM_001350021.2:c.-133-5121T>A	NP_001336950.1:n.-133-5121T>A
NM_001350022.2:c.282-5121T>A	NP_001336951.1:n.282-5121T>A