Canonical Allele Identifier: CA4839821

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 544219
• ClinVar RCV Id: RCV000655307 ; RCV001354602
• dbSNP Id: rs34248551
• ExAC: 8:106814181 C / G
• gnomAD v2: 8-106814181-C-G
• gnomAD v3: 8-105801953-C-G
• gnomAD v4: 8-105801953-C-G
• MyVariant Identifiers: chr8:g.106814181C>G (hg19) ; chr8:g.105801953C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801953C>G , CM000670.2:g.105801953C>G	GRCh38
NC_000008.10:g.106814181C>G , CM000670.1:g.106814181C>G	GRCh37
NC_000008.9:g.106883357C>G	NCBI36
NG_011723.1:g.488035C>G
NG_011723.2:g.488035C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000407775.7:c.1871C>G (ZFPM2) MANE Select	ENSP00000384179.2:p.Ser624Cys
ENST00000407775.6:c.1871C>G (ZFPM2)	ENSP00000384179.2:p.Ser624Cys
ENST00000517361.1:c.1475C>G (ZFPM2)	ENSP00000428720.1:p.Ser492Cys
ENST00000520492.5:c.1475C>G (ZFPM2)	ENSP00000430757.1:p.Ser492Cys
ENST00000522296.1:n.1665C>G (ZFPM2)
NM_012082.3:c.1871C>G (ZFPM2)	NP_036214.2:p.Ser624Cys
NR_125796.1:n.180-3511G>C (ZFPM2-AS1)
NR_125797.1:n.191-3511G>C (ZFPM2-AS1)
XM_011516946.1:c.1910C>G (ZFPM2)	XP_011515248.1:p.Ser637Cys
XM_011516947.1:c.1841C>G (ZFPM2)	XP_011515249.1:p.Ser614Cys
XM_011516948.1:c.1712C>G (ZFPM2)	XP_011515250.1:p.Ser571Cys
XM_011516949.1:c.1703C>G (ZFPM2)	XP_011515251.1:p.Ser568Cys
NM_001362836.1:c.1712C>G (ZFPM2)	NP_001349765.1:p.Ser571Cys
NM_001362837.1:c.1475C>G (ZFPM2)	NP_001349766.1:p.Ser492Cys
XM_011516947.3:c.1841C>G (ZFPM2)	XP_011515249.1:p.Ser614Cys
NM_012082.4:c.1871C>G (ZFPM2) MANE Select	NP_036214.2:p.Ser624Cys
NM_001362836.2:c.1712C>G (ZFPM2)	NP_001349765.1:p.Ser571Cys
NM_001362837.2:c.1475C>G (ZFPM2)	NP_001349766.1:p.Ser492Cys