Canonical Allele Identifier: CA393364447
Gene: ZNF592 HGNC NCBI

Linked Data

dbSNP Id: rs1298587907

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