Canonical Allele Identifier: CA393364430

Gene: ZNF592

Linked Data

• MyVariant Identifiers: chr15:g.85342368T>G (hg19) ; chr15:g.84799137T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799137T>G , CM000677.2:g.84799137T>G	GRCh38
NC_000015.9:g.85342368T>G , CM000677.1:g.85342368T>G	GRCh37
NC_000015.8:g.83143372T>G	NCBI36
NG_028094.1:g.55551T>G
NG_028094.2:g.55551T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560079.7:c.3064T>G MANE Select	ENSP00000452877.2:p.Phe1022Val
ENST00000299927.4:c.3064T>G	ENSP00000299927.3:p.Phe1022Val
ENST00000559607.1:c.*476T>G	ENSP00000453491.1:n.*476T>G
ENST00000560079.6:c.3064T>G	ENSP00000452877.2:p.Phe1022Val
NM_014630.2:c.3064T>G	NP_055445.2:p.Phe1022Val
XM_005254996.2:c.3064T>G	XP_005255053.1:p.Phe1022Val
XM_011522246.1:c.3064T>G	XP_011520548.1:p.Phe1022Val
XM_011522247.1:c.3064T>G	XP_011520549.1:p.Phe1022Val
XM_011522248.1:c.3064T>G	XP_011520550.1:p.Phe1022Val
XR_931951.1:n.3452T>G
XM_005254996.3:c.3064T>G	XP_005255053.1:p.Phe1022Val
XM_011522246.2:c.3064T>G	XP_011520548.1:p.Phe1022Val
XM_011522247.2:c.3064T>G	XP_011520549.1:p.Phe1022Val
XM_011522248.2:c.3064T>G	XP_011520550.1:p.Phe1022Val
XM_017022734.1:c.3064T>G	XP_016878223.1:p.Phe1022Val
XR_931951.2:n.3457T>G
NM_014630.3:c.3064T>G MANE Select	NP_055445.2:p.Phe1022Val