Canonical Allele Identifier: CA182650064

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 2315739
• ClinVar RCV Id: RCV002888413
• dbSNP Id: rs371103322
• gnomAD v2: 8-106814285-A-G
• gnomAD v3: 8-105802057-A-G
• gnomAD v4: 8-105802057-A-G
• MyVariant Identifiers: chr8:g.106814285A>G (hg19) ; chr8:g.106814285_106814288delinsGATG (hg19) ; chr8:g.105802057A>G (hg38) ; chr8:g.105802057_105802060delinsGATG (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000407775.7:c.1975A>G (ZFPM2) MANE Select	ENSP00000384179.2:p.Asn659Asp
ENST00000407775.6:c.1975A>G (ZFPM2)	ENSP00000384179.2:p.Asn659Asp
ENST00000517361.1:c.1579A>G (ZFPM2)	ENSP00000428720.1:p.Asn527Asp
ENST00000520492.5:c.1579A>G (ZFPM2)	ENSP00000430757.1:p.Asn527Asp
ENST00000522296.1:n.1769A>G (ZFPM2)
NM_012082.3:c.1975A>G (ZFPM2)	NP_036214.2:p.Asn659Asp
NR_125796.1:n.180-3615T>C (ZFPM2-AS1)
NR_125797.1:n.191-3615T>C (ZFPM2-AS1)
XM_011516946.1:c.2014A>G (ZFPM2)	XP_011515248.1:p.Asn672Asp
XM_011516947.1:c.1945A>G (ZFPM2)	XP_011515249.1:p.Asn649Asp
XM_011516948.1:c.1816A>G (ZFPM2)	XP_011515250.1:p.Asn606Asp
XM_011516949.1:c.1807A>G (ZFPM2)	XP_011515251.1:p.Asn603Asp
NM_001362836.1:c.1816A>G (ZFPM2)	NP_001349765.1:p.Asn606Asp
NM_001362837.1:c.1579A>G (ZFPM2)	NP_001349766.1:p.Asn527Asp
XM_011516947.3:c.1945A>G (ZFPM2)	XP_011515249.1:p.Asn649Asp
NM_012082.4:c.1975A>G (ZFPM2) MANE Select	NP_036214.2:p.Asn659Asp
NM_001362836.2:c.1816A>G (ZFPM2)	NP_001349765.1:p.Asn606Asp
NM_001362837.2:c.1579A>G (ZFPM2)	NP_001349766.1:p.Asn527Asp