Canonical Allele Identifier: CA2840620172

Gene: ZNF592

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799306del , CM000677.2:g.84799306del	GRCh38
NC_000015.9:g.85342537del , CM000677.1:g.85342537del	GRCh37
NC_000015.8:g.83143541del	NCBI36
NG_028094.1:g.55720del
NG_028094.2:g.55720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560079.7:c.3137+96del MANE Select	ENSP00000452877.2:n.3137+96del
ENST00000299927.4:c.3137+96del	ENSP00000299927.3:n.3137+96del
ENST00000559607.1:c.*549+96del	ENSP00000453491.1:n.*549+96del
ENST00000560079.6:c.3137+96del	ENSP00000452877.2:n.3137+96del
NM_014630.2:c.3137+96del	NP_055445.2:n.3137+96del
XM_005254996.2:c.3137+96del	XP_005255053.1:n.3137+96del
XM_011522246.1:c.3137+96del	XP_011520548.1:n.3137+96del
XM_011522247.1:c.3137+96del	XP_011520549.1:n.3137+96del
XM_011522248.1:c.3137+96del	XP_011520550.1:n.3137+96del
XR_931951.1:n.3525+96del
XM_005254996.3:c.3137+96del	XP_005255053.1:n.3137+96del
XM_011522246.2:c.3137+96del	XP_011520548.1:n.3137+96del
XM_011522247.2:c.3137+96del	XP_011520549.1:n.3137+96del
XM_011522248.2:c.3137+96del	XP_011520550.1:n.3137+96del
XM_017022734.1:c.3137+96del	XP_016878223.1:n.3137+96del
XR_931951.2:n.3530+96del
NM_014630.3:c.3137+96del MANE Select	NP_055445.2:n.3137+96del