Canonical Allele Identifier: CA4839771

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 544224
• ClinVar RCV Id: RCV000655312 ; RCV003432714
• dbSNP Id: rs200643137
• ExAC: 8:106813888 G / T
• gnomAD v2: 8-106813888-G-T
• gnomAD v3: 8-105801660-G-T
• gnomAD v4: 8-105801660-G-T
• MyVariant Identifiers: chr8:g.106813888G>T (hg19) ; chr8:g.105801660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801660G>T , CM000670.2:g.105801660G>T	GRCh38
NC_000008.10:g.106813888G>T , CM000670.1:g.106813888G>T	GRCh37
NC_000008.9:g.106883064G>T	NCBI36
NG_011723.1:g.487742G>T
NG_011723.2:g.487742G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1578G>T (ZFPM2) MANE Select	ENSP00000384179.2:p.Arg526=
ENST00000407775.6:c.1578G>T (ZFPM2)	ENSP00000384179.2:p.Arg526=
ENST00000517361.1:c.1182G>T (ZFPM2)	ENSP00000428720.1:p.Arg394=
ENST00000520492.5:c.1182G>T (ZFPM2)	ENSP00000430757.1:p.Arg394=
ENST00000522296.1:n.1372G>T (ZFPM2)
NM_012082.3:c.1578G>T (ZFPM2)	NP_036214.2:p.Arg526=
NR_125796.1:n.180-3218C>A (ZFPM2-AS1)
NR_125797.1:n.191-3218C>A (ZFPM2-AS1)
XM_011516946.1:c.1617G>T (ZFPM2)	XP_011515248.1:p.Arg539=
XM_011516947.1:c.1548G>T (ZFPM2)	XP_011515249.1:p.Arg516=
XM_011516948.1:c.1419G>T (ZFPM2)	XP_011515250.1:p.Arg473=
XM_011516949.1:c.1410G>T (ZFPM2)	XP_011515251.1:p.Arg470=
NM_001362836.1:c.1419G>T (ZFPM2)	NP_001349765.1:p.Arg473=
NM_001362837.1:c.1182G>T (ZFPM2)	NP_001349766.1:p.Arg394=
XM_011516947.3:c.1548G>T (ZFPM2)	XP_011515249.1:p.Arg516=
NM_012082.4:c.1578G>T (ZFPM2) MANE Select	NP_036214.2:p.Arg526=
NM_001362836.2:c.1419G>T (ZFPM2)	NP_001349765.1:p.Arg473=
NM_001362837.2:c.1182G>T (ZFPM2)	NP_001349766.1:p.Arg394=