Canonical Allele Identifier: CA2192351988

Gene: ZNF592

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799229T= , CM000677.2:g.84799229T=	GRCh38
NC_000015.9:g.85342460T= , CM000677.1:g.85342460T=	GRCh37
NC_000015.8:g.83143464T=	NCBI36
NG_028094.1:g.55643T=
NG_028094.2:g.55643T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560079.7:c.3137+19T= MANE Select	ENSP00000452877.2:n.3137+19T=
ENST00000299927.4:c.3137+19T=	ENSP00000299927.3:n.3137+19T=
ENST00000559607.1:c.*549+19T=	ENSP00000453491.1:n.*549+19T=
ENST00000560079.6:c.3137+19T=	ENSP00000452877.2:n.3137+19T=
NM_014630.2:c.3137+19T=	NP_055445.2:n.3137+19T=
XM_005254996.2:c.3137+19T=	XP_005255053.1:n.3137+19T=
XM_011522246.1:c.3137+19T=	XP_011520548.1:n.3137+19T=
XM_011522247.1:c.3137+19T=	XP_011520549.1:n.3137+19T=
XM_011522248.1:c.3137+19T=	XP_011520550.1:n.3137+19T=
XR_931951.1:n.3525+19T=
XM_005254996.3:c.3137+19T=	XP_005255053.1:n.3137+19T=
XM_011522246.2:c.3137+19T=	XP_011520548.1:n.3137+19T=
XM_011522247.2:c.3137+19T=	XP_011520549.1:n.3137+19T=
XM_011522248.2:c.3137+19T=	XP_011520550.1:n.3137+19T=
XM_017022734.1:c.3137+19T=	XP_016878223.1:n.3137+19T=
XR_931951.2:n.3530+19T=
NM_014630.3:c.3137+19T= MANE Select	NP_055445.2:n.3137+19T=