Canonical Allele Identifier: CA4839837

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 1338377
• ClinVar RCV Id: RCV001817748
• dbSNP Id: rs759533183
• ExAC: 8:106814284 CAAT / C
• gnomAD v2: 8-106814284-CAAT-C
• gnomAD v3: 8-105802056-CAAT-C
• gnomAD v4: 8-105802056-CAAT-C
• MyVariant Identifiers: chr8:g.106814285_106814287del (hg19) ; chr8:g.105802057_105802059del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105802057_105802059del , CM000670.2:g.105802057_105802059del	GRCh38
NC_000008.10:g.106814285_106814287del , CM000670.1:g.106814285_106814287del	GRCh37
NC_000008.9:g.106883461_106883463del	NCBI36
NG_011723.1:g.488139_488141del
NG_011723.2:g.488139_488141del

Transcript Alleles

HGVS	Amino-acid change
ENST00000407775.7:c.1975_1977del (ZFPM2) MANE Select	ENSP00000384179.2:p.Asn659del
ENST00000407775.6:c.1975_1977del (ZFPM2)	ENSP00000384179.2:p.Asn659del
ENST00000517361.1:c.1579_1581del (ZFPM2)	ENSP00000428720.1:p.Asn527del
ENST00000520492.5:c.1579_1581del (ZFPM2)	ENSP00000430757.1:p.Asn527del
ENST00000522296.1:n.1769_1771del (ZFPM2)
NM_012082.3:c.1975_1977del (ZFPM2)	NP_036214.2:p.Asn659del
NR_125796.1:n.180-3617_180-3615del (ZFPM2-AS1)
NR_125797.1:n.191-3617_191-3615del (ZFPM2-AS1)
XM_011516946.1:c.2014_2016del (ZFPM2)	XP_011515248.1:p.Asn672del
XM_011516947.1:c.1945_1947del (ZFPM2)	XP_011515249.1:p.Asn649del
XM_011516948.1:c.1816_1818del (ZFPM2)	XP_011515250.1:p.Asn606del
XM_011516949.1:c.1807_1809del (ZFPM2)	XP_011515251.1:p.Asn603del
NM_001362836.1:c.1816_1818del (ZFPM2)	NP_001349765.1:p.Asn606del
NM_001362837.1:c.1579_1581del (ZFPM2)	NP_001349766.1:p.Asn527del
XM_011516947.3:c.1945_1947del (ZFPM2)	XP_011515249.1:p.Asn649del
NM_012082.4:c.1975_1977del (ZFPM2) MANE Select	NP_036214.2:p.Asn659del
NM_001362836.2:c.1816_1818del (ZFPM2)	NP_001349765.1:p.Asn606del
NM_001362837.2:c.1579_1581del (ZFPM2)	NP_001349766.1:p.Asn527del