Canonical Allele Identifier: CA393364599

Gene: ZNF592

Linked Data

• gnomAD v4: 15-84799212-T-A
• MyVariant Identifiers: chr15:g.85342443T>A (hg19) ; chr15:g.84799212T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799212T>A , CM000677.2:g.84799212T>A	GRCh38
NC_000015.9:g.85342443T>A , CM000677.1:g.85342443T>A	GRCh37
NC_000015.8:g.83143447T>A	NCBI36
NG_028094.1:g.55626T>A
NG_028094.2:g.55626T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560079.7:c.3137+2T>A MANE Select	ENSP00000452877.2:n.3137+2T>A
ENST00000299927.4:c.3137+2T>A	ENSP00000299927.3:n.3137+2T>A
ENST00000559607.1:c.*549+2T>A	ENSP00000453491.1:n.*549+2T>A
ENST00000560079.6:c.3137+2T>A	ENSP00000452877.2:n.3137+2T>A
NM_014630.2:c.3137+2T>A	NP_055445.2:n.3137+2T>A
XM_005254996.2:c.3137+2T>A	XP_005255053.1:n.3137+2T>A
XM_011522246.1:c.3137+2T>A	XP_011520548.1:n.3137+2T>A
XM_011522247.1:c.3137+2T>A	XP_011520549.1:n.3137+2T>A
XM_011522248.1:c.3137+2T>A	XP_011520550.1:n.3137+2T>A
XR_931951.1:n.3525+2T>A
XM_005254996.3:c.3137+2T>A	XP_005255053.1:n.3137+2T>A
XM_011522246.2:c.3137+2T>A	XP_011520548.1:n.3137+2T>A
XM_011522247.2:c.3137+2T>A	XP_011520549.1:n.3137+2T>A
XM_011522248.2:c.3137+2T>A	XP_011520550.1:n.3137+2T>A
XM_017022734.1:c.3137+2T>A	XP_016878223.1:n.3137+2T>A
XR_931951.2:n.3530+2T>A
NM_014630.3:c.3137+2T>A MANE Select	NP_055445.2:n.3137+2T>A