Canonical Allele Identifier: CA7708575

Gene: ZNF592

Linked Data

• dbSNP Id: rs1555432283
• ExAC: 15:85342447 T / C
• gnomAD v2: 15-85342447-T-C
• gnomAD v3: 15-84799216-T-C
• gnomAD v4: 15-84799216-T-C
• MyVariant Identifiers: chr15:g.85342447T>C (hg19) ; chr15:g.85342447_85342448delinsCC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.84799216T>C , CM000677.2:g.84799216T>C	GRCh38
NC_000015.9:g.85342447T>C , CM000677.1:g.85342447T>C	GRCh37
NC_000015.8:g.83143451T>C	NCBI36
NG_028094.1:g.55630T>C
NG_028094.2:g.55630T>C

Transcript Alleles

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