Canonical Allele Identifier: CA492276298

Gene: ZNF592

Linked Data

• MyVariant Identifiers: chr15:g.85342421A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799190A>C , CM000677.2:g.84799190A>C	GRCh38
NC_000015.9:g.85342421A>C , CM000677.1:g.85342421A>C	GRCh37
NC_000015.8:g.83143425A>C	NCBI36
NG_028094.1:g.55604A>C
NG_028094.2:g.55604A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560079.7:c.3117A>C MANE Select	ENSP00000452877.2:p.Val1039=
ENST00000299927.4:c.3117A>C	ENSP00000299927.3:p.Val1039=
ENST00000559607.1:c.*529A>C	ENSP00000453491.1:n.*529A>C
ENST00000560079.6:c.3117A>C	ENSP00000452877.2:p.Val1039=
NM_014630.2:c.3117A>C	NP_055445.2:p.Val1039=
XM_005254996.2:c.3117A>C	XP_005255053.1:p.Val1039=
XM_011522246.1:c.3117A>C	XP_011520548.1:p.Val1039=
XM_011522247.1:c.3117A>C	XP_011520549.1:p.Val1039=
XM_011522248.1:c.3117A>C	XP_011520550.1:p.Val1039=
XR_931951.1:n.3505A>C
XM_005254996.3:c.3117A>C	XP_005255053.1:p.Val1039=
XM_011522246.2:c.3117A>C	XP_011520548.1:p.Val1039=
XM_011522247.2:c.3117A>C	XP_011520549.1:p.Val1039=
XM_011522248.2:c.3117A>C	XP_011520550.1:p.Val1039=
XM_017022734.1:c.3117A>C	XP_016878223.1:p.Val1039=
XR_931951.2:n.3510A>C
NM_014630.3:c.3117A>C MANE Select	NP_055445.2:p.Val1039=