Canonical Allele Identifier: CA4839775

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 2142043
• ClinVar RCV Id: RCV003058855 ; RCV003058856
• dbSNP Id: rs768867827
• ExAC: 8:106813902 G / A
• gnomAD v2: 8-106813902-G-A
• gnomAD v3: 8-105801674-G-A
• gnomAD v4: 8-105801674-G-A
• COSMIC: COSM3271123
• MyVariant Identifiers: chr8:g.106813902G>A (hg19) ; chr8:g.105801674G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801674G>A , CM000670.2:g.105801674G>A	GRCh38
NC_000008.10:g.106813902G>A , CM000670.1:g.106813902G>A	GRCh37
NC_000008.9:g.106883078G>A	NCBI36
NG_011723.1:g.487756G>A
NG_011723.2:g.487756G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1592G>A (ZFPM2) MANE Select	ENSP00000384179.2:p.Gly531Asp
ENST00000407775.6:c.1592G>A (ZFPM2)	ENSP00000384179.2:p.Gly531Asp
ENST00000517361.1:c.1196G>A (ZFPM2)	ENSP00000428720.1:p.Gly399Asp
ENST00000520492.5:c.1196G>A (ZFPM2)	ENSP00000430757.1:p.Gly399Asp
ENST00000522296.1:n.1386G>A (ZFPM2)
NM_012082.3:c.1592G>A (ZFPM2)	NP_036214.2:p.Gly531Asp
NR_125796.1:n.180-3232C>T (ZFPM2-AS1)
NR_125797.1:n.191-3232C>T (ZFPM2-AS1)
XM_011516946.1:c.1631G>A (ZFPM2)	XP_011515248.1:p.Gly544Asp
XM_011516947.1:c.1562G>A (ZFPM2)	XP_011515249.1:p.Gly521Asp
XM_011516948.1:c.1433G>A (ZFPM2)	XP_011515250.1:p.Gly478Asp
XM_011516949.1:c.1424G>A (ZFPM2)	XP_011515251.1:p.Gly475Asp
NM_001362836.1:c.1433G>A (ZFPM2)	NP_001349765.1:p.Gly478Asp
NM_001362837.1:c.1196G>A (ZFPM2)	NP_001349766.1:p.Gly399Asp
XM_011516947.3:c.1562G>A (ZFPM2)	XP_011515249.1:p.Gly521Asp
NM_012082.4:c.1592G>A (ZFPM2) MANE Select	NP_036214.2:p.Gly531Asp
NM_001362836.2:c.1433G>A (ZFPM2)	NP_001349765.1:p.Gly478Asp
NM_001362837.2:c.1196G>A (ZFPM2)	NP_001349766.1:p.Gly399Asp