Canonical Allele Identifier: CA2192351930

Gene: ZNF592

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799201A= , CM000677.2:g.84799201A=	GRCh38
NC_000015.9:g.85342432A= , CM000677.1:g.85342432A=	GRCh37
NC_000015.8:g.83143436A=	NCBI36
NG_028094.1:g.55615A=
NG_028094.2:g.55615A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560079.7:c.3128A= MANE Select	ENSP00000452877.2:p.Tyr1043=
ENST00000299927.4:c.3128A=	ENSP00000299927.3:p.Tyr1043=
ENST00000559607.1:c.*540A=	ENSP00000453491.1:n.*540A=
ENST00000560079.6:c.3128A=	ENSP00000452877.2:p.Tyr1043=
NM_014630.2:c.3128A=	NP_055445.2:p.Tyr1043=
XM_005254996.2:c.3128A=	XP_005255053.1:p.Tyr1043=
XM_011522246.1:c.3128A=	XP_011520548.1:p.Tyr1043=
XM_011522247.1:c.3128A=	XP_011520549.1:p.Tyr1043=
XM_011522248.1:c.3128A=	XP_011520550.1:p.Tyr1043=
XR_931951.1:n.3516A=
XM_005254996.3:c.3128A=	XP_005255053.1:p.Tyr1043=
XM_011522246.2:c.3128A=	XP_011520548.1:p.Tyr1043=
XM_011522247.2:c.3128A=	XP_011520549.1:p.Tyr1043=
XM_011522248.2:c.3128A=	XP_011520550.1:p.Tyr1043=
XM_017022734.1:c.3128A=	XP_016878223.1:p.Tyr1043=
XR_931951.2:n.3521A=
NM_014630.3:c.3128A= MANE Select	NP_055445.2:p.Tyr1043=