Canonical Allele Identifier: CA2838327831

Gene: ZNF329

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.58154715del , CM000681.2:g.58154715del	GRCh38
NC_000019.9:g.58666082del , CM000681.1:g.58666082del	GRCh37
NC_000019.8:g.63357894del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000500161.2:c.-208+20del	ENSP00000439527.1:n.-208+20del
ENST00000601887.1:c.-9+20del	ENSP00000471614.1:n.-9+20del
XM_006723384.2:c.-9+20del	XP_006723447.1:n.-9+20del
XM_011527310.1:c.-177+20del	XP_011525612.1:n.-177+20del
XM_011527313.1:c.-83+20del	XP_011525615.1:n.-83+20del
XM_011527315.1:c.-208+20del	XP_011525617.1:n.-208+20del
XM_006723383.3:c.-296del	XP_006723446.1:n.-296del
XM_006723384.3:c.-9+20del	XP_006723447.1:n.-9+20del
XM_011527310.2:c.-177+20del	XP_011525612.1:n.-177+20del
XM_011527311.2:c.-370del	XP_011525613.1:n.-370del
XM_011527313.2:c.-83+20del	XP_011525615.1:n.-83+20del
XM_011527314.2:c.-426del	XP_011525616.1:n.-426del
XM_017027307.1:c.-495del	XP_016882796.1:n.-495del
XM_017027308.1:c.-401del	XP_016882797.1:n.-401del
XM_017027309.1:c.-114+20del	XP_016882798.1:n.-114+20del
XM_017027310.1:c.-457del	XP_016882799.1:n.-457del
XM_017027311.1:c.-352del	XP_016882800.1:n.-352del