Canonical Allele Identifier: CA492276326

Gene: ZNF592

Linked Data

• gnomAD v4: 15-84799205-C-T
• MyVariant Identifiers: chr15:g.85342436C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799205C>T , CM000677.2:g.84799205C>T	GRCh38
NC_000015.9:g.85342436C>T , CM000677.1:g.85342436C>T	GRCh37
NC_000015.8:g.83143440C>T	NCBI36
NG_028094.1:g.55619C>T
NG_028094.2:g.55619C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560079.7:c.3132C>T MANE Select	ENSP00000452877.2:p.Thr1044=
ENST00000299927.4:c.3132C>T	ENSP00000299927.3:p.Thr1044=
ENST00000559607.1:c.*544C>T	ENSP00000453491.1:n.*544C>T
ENST00000560079.6:c.3132C>T	ENSP00000452877.2:p.Thr1044=
NM_014630.2:c.3132C>T	NP_055445.2:p.Thr1044=
XM_005254996.2:c.3132C>T	XP_005255053.1:p.Thr1044=
XM_011522246.1:c.3132C>T	XP_011520548.1:p.Thr1044=
XM_011522247.1:c.3132C>T	XP_011520549.1:p.Thr1044=
XM_011522248.1:c.3132C>T	XP_011520550.1:p.Thr1044=
XR_931951.1:n.3520C>T
XM_005254996.3:c.3132C>T	XP_005255053.1:p.Thr1044=
XM_011522246.2:c.3132C>T	XP_011520548.1:p.Thr1044=
XM_011522247.2:c.3132C>T	XP_011520549.1:p.Thr1044=
XM_011522248.2:c.3132C>T	XP_011520550.1:p.Thr1044=
XM_017022734.1:c.3132C>T	XP_016878223.1:p.Thr1044=
XR_931951.2:n.3525C>T
NM_014630.3:c.3132C>T MANE Select	NP_055445.2:p.Thr1044=