Canonical Allele Identifier: CA1431538879

Gene: ZDHHC19

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.196201983G= , CM000665.2:g.196201983G=	GRCh38
NC_000003.11:g.195928854G= , CM000665.1:g.195928854G=	GRCh37
NC_000003.10:g.197413251G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296326.8:c.688-3109C= MANE Select	ENSP00000296326.3:n.688-3109C=
ENST00000296326.7:c.688-3109C=	ENSP00000296326.3:n.688-3109C=
ENST00000397544.6:c.688-3109C=	ENSP00000380678.2:n.688-3109C=
ENST00000438232.5:c.688-2461C=	ENSP00000393710.1:n.688-2461C=
ENST00000465519.5:n.1283-3114C=
NM_001039617.1:c.688-3109C=	NP_001034706.1:n.688-3109C=
XM_005269277.3:c.688-3109C=	XP_005269334.1:n.688-3109C=
XM_005269278.3:c.688-3114C=	XP_005269335.1:n.688-3114C=
XM_005269279.2:c.688-3532C=	XP_005269336.1:n.688-3532C=
XM_006713493.2:c.682-3109C=	XP_006713556.1:n.682-3109C=
XM_006713494.2:c.610-3109C=	XP_006713557.1:n.610-3109C=
XM_011512414.1:c.688-3109C=	XP_011510716.1:n.688-3109C=
XM_011512415.1:c.688-3114C=	XP_011510717.1:n.688-3114C=
XM_011512416.1:c.523-3109C=	XP_011510718.1:n.523-3109C=
XM_011512417.1:c.466-3109C=	XP_011510719.1:n.466-3109C=
XR_246038.2:n.810-3114C=
XR_924098.1:n.810-3109C=
XR_924099.1:n.810-2461C=
XR_924100.1:n.810-2461C=
NR_135617.1:n.810-2461C=
NR_135618.1:n.810-3109C=
XM_005269279.3:c.688-3532C=	XP_005269336.1:n.688-3532C=
XR_001740011.1:n.810-3114C=
XR_001740012.1:n.810-3109C=
XR_001740013.1:n.810-3114C=
XR_002959490.1:n.720-2461C=
NM_001039617.2:c.688-3109C= MANE Select	NP_001034706.1:n.688-3109C=
NR_135617.2:n.773-2461C=
NR_135618.2:n.773-3109C=