Canonical Allele Identifier: CA393364447

Gene: ZNF592

Linked Data

• dbSNP Id: rs1298587907
• gnomAD v2: 15-85342377-C-A
• gnomAD v4: 15-84799146-C-A
• MyVariant Identifiers: chr15:g.85342377C>A (hg19) ; chr15:g.84799146C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799146C>A , CM000677.2:g.84799146C>A	GRCh38
NC_000015.9:g.85342377C>A , CM000677.1:g.85342377C>A	GRCh37
NC_000015.8:g.83143381C>A	NCBI36
NG_028094.1:g.55560C>A
NG_028094.2:g.55560C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560079.7:c.3073C>A MANE Select	ENSP00000452877.2:p.Pro1025Thr
ENST00000299927.4:c.3073C>A	ENSP00000299927.3:p.Pro1025Thr
ENST00000559607.1:c.*485C>A	ENSP00000453491.1:n.*485C>A
ENST00000560079.6:c.3073C>A	ENSP00000452877.2:p.Pro1025Thr
NM_014630.2:c.3073C>A	NP_055445.2:p.Pro1025Thr
XM_005254996.2:c.3073C>A	XP_005255053.1:p.Pro1025Thr
XM_011522246.1:c.3073C>A	XP_011520548.1:p.Pro1025Thr
XM_011522247.1:c.3073C>A	XP_011520549.1:p.Pro1025Thr
XM_011522248.1:c.3073C>A	XP_011520550.1:p.Pro1025Thr
XR_931951.1:n.3461C>A
XM_005254996.3:c.3073C>A	XP_005255053.1:p.Pro1025Thr
XM_011522246.2:c.3073C>A	XP_011520548.1:p.Pro1025Thr
XM_011522247.2:c.3073C>A	XP_011520549.1:p.Pro1025Thr
XM_011522248.2:c.3073C>A	XP_011520550.1:p.Pro1025Thr
XM_017022734.1:c.3073C>A	XP_016878223.1:p.Pro1025Thr
XR_931951.2:n.3466C>A
NM_014630.3:c.3073C>A MANE Select	NP_055445.2:p.Pro1025Thr