Canonical Allele Identifier: CA2192352000

Gene: ZNF592

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799236G= , CM000677.2:g.84799236G=	GRCh38
NC_000015.9:g.85342467G= , CM000677.1:g.85342467G=	GRCh37
NC_000015.8:g.83143471G=	NCBI36
NG_028094.1:g.55650G=
NG_028094.2:g.55650G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560079.7:c.3137+26G= MANE Select	ENSP00000452877.2:n.3137+26G=
ENST00000299927.4:c.3137+26G=	ENSP00000299927.3:n.3137+26G=
ENST00000559607.1:c.*549+26G=	ENSP00000453491.1:n.*549+26G=
ENST00000560079.6:c.3137+26G=	ENSP00000452877.2:n.3137+26G=
NM_014630.2:c.3137+26G=	NP_055445.2:n.3137+26G=
XM_005254996.2:c.3137+26G=	XP_005255053.1:n.3137+26G=
XM_011522246.1:c.3137+26G=	XP_011520548.1:n.3137+26G=
XM_011522247.1:c.3137+26G=	XP_011520549.1:n.3137+26G=
XM_011522248.1:c.3137+26G=	XP_011520550.1:n.3137+26G=
XR_931951.1:n.3525+26G=
XM_005254996.3:c.3137+26G=	XP_005255053.1:n.3137+26G=
XM_011522246.2:c.3137+26G=	XP_011520548.1:n.3137+26G=
XM_011522247.2:c.3137+26G=	XP_011520549.1:n.3137+26G=
XM_011522248.2:c.3137+26G=	XP_011520550.1:n.3137+26G=
XM_017022734.1:c.3137+26G=	XP_016878223.1:n.3137+26G=
XR_931951.2:n.3530+26G=
NM_014630.3:c.3137+26G= MANE Select	NP_055445.2:n.3137+26G=