Canonical Allele Identifier: CA4839839

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 2514223
• ClinVar RCV Id: RCV003244987
• dbSNP Id: rs371103322
• ExAC: 8:106814285 A / C
• gnomAD v2: 8-106814285-A-C
• gnomAD v4: 8-105802057-A-C
• MyVariant Identifiers: chr8:g.106814285A>C (hg19) ; chr8:g.106814285_106814288delinsCATG (hg19) ; chr8:g.105802057A>C (hg38) ; chr8:g.105802057_105802060delinsCATG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105802057A>C , CM000670.2:g.105802057A>C	GRCh38
NC_000008.10:g.106814285A>C , CM000670.1:g.106814285A>C	GRCh37
NC_000008.9:g.106883461A>C	NCBI36
NG_011723.1:g.488139A>C
NG_011723.2:g.488139A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000407775.7:c.1975A>C (ZFPM2) MANE Select	ENSP00000384179.2:p.Asn659His
ENST00000407775.6:c.1975A>C (ZFPM2)	ENSP00000384179.2:p.Asn659His
ENST00000517361.1:c.1579A>C (ZFPM2)	ENSP00000428720.1:p.Asn527His
ENST00000520492.5:c.1579A>C (ZFPM2)	ENSP00000430757.1:p.Asn527His
ENST00000522296.1:n.1769A>C (ZFPM2)
NM_012082.3:c.1975A>C (ZFPM2)	NP_036214.2:p.Asn659His
NR_125796.1:n.180-3615T>G (ZFPM2-AS1)
NR_125797.1:n.191-3615T>G (ZFPM2-AS1)
XM_011516946.1:c.2014A>C (ZFPM2)	XP_011515248.1:p.Asn672His
XM_011516947.1:c.1945A>C (ZFPM2)	XP_011515249.1:p.Asn649His
XM_011516948.1:c.1816A>C (ZFPM2)	XP_011515250.1:p.Asn606His
XM_011516949.1:c.1807A>C (ZFPM2)	XP_011515251.1:p.Asn603His
NM_001362836.1:c.1816A>C (ZFPM2)	NP_001349765.1:p.Asn606His
NM_001362837.1:c.1579A>C (ZFPM2)	NP_001349766.1:p.Asn527His
XM_011516947.3:c.1945A>C (ZFPM2)	XP_011515249.1:p.Asn649His
NM_012082.4:c.1975A>C (ZFPM2) MANE Select	NP_036214.2:p.Asn659His
NM_001362836.2:c.1816A>C (ZFPM2)	NP_001349765.1:p.Asn606His
NM_001362837.2:c.1579A>C (ZFPM2)	NP_001349766.1:p.Asn527His