Canonical Allele Identifier: CA2570229869

Gene: ZNF592

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799276G>T , CM000677.2:g.84799276G>T	GRCh38
NC_000015.9:g.85342507G>T , CM000677.1:g.85342507G>T	GRCh37
NC_000015.8:g.83143511G>T	NCBI36
NG_028094.1:g.55690G>T
NG_028094.2:g.55690G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000560079.7:c.3137+66G>T MANE Select	ENSP00000452877.2:n.3137+66G>T
ENST00000299927.4:c.3137+66G>T	ENSP00000299927.3:n.3137+66G>T
ENST00000559607.1:c.*549+66G>T	ENSP00000453491.1:n.*549+66G>T
ENST00000560079.6:c.3137+66G>T	ENSP00000452877.2:n.3137+66G>T
NM_014630.2:c.3137+66G>T	NP_055445.2:n.3137+66G>T
XM_005254996.2:c.3137+66G>T	XP_005255053.1:n.3137+66G>T
XM_011522246.1:c.3137+66G>T	XP_011520548.1:n.3137+66G>T
XM_011522247.1:c.3137+66G>T	XP_011520549.1:n.3137+66G>T
XM_011522248.1:c.3137+66G>T	XP_011520550.1:n.3137+66G>T
XR_931951.1:n.3525+66G>T
XM_005254996.3:c.3137+66G>T	XP_005255053.1:n.3137+66G>T
XM_011522246.2:c.3137+66G>T	XP_011520548.1:n.3137+66G>T
XM_011522247.2:c.3137+66G>T	XP_011520549.1:n.3137+66G>T
XM_011522248.2:c.3137+66G>T	XP_011520550.1:n.3137+66G>T
XM_017022734.1:c.3137+66G>T	XP_016878223.1:n.3137+66G>T
XR_931951.2:n.3530+66G>T
NM_014630.3:c.3137+66G>T MANE Select	NP_055445.2:n.3137+66G>T