Canonical Allele Identifier: CA2579226009

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 1320815
• ClinVar RCV Id: RCV001776794
• dbSNP Id: rs2131178384

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801757_105801759del , CM000670.2:g.105801757_105801759del	GRCh38
NC_000008.10:g.106813985_106813987del , CM000670.1:g.106813985_106813987del	GRCh37
NC_000008.9:g.106883161_106883163del	NCBI36
NG_011723.1:g.487839_487841del
NG_011723.2:g.487839_487841del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1675_1677del (ZFPM2) MANE Select	ENSP00000384179.2:p.Asn559del
ENST00000407775.6:c.1675_1677del (ZFPM2)	ENSP00000384179.2:p.Asn559del
ENST00000517361.1:c.1279_1281del (ZFPM2)	ENSP00000428720.1:p.Asn427del
ENST00000520492.5:c.1279_1281del (ZFPM2)	ENSP00000430757.1:p.Asn427del
ENST00000522296.1:n.1469_1471del (ZFPM2)
NM_012082.3:c.1675_1677del (ZFPM2)	NP_036214.2:p.Asn559del
NR_125796.1:n.180-3314_180-3312del (ZFPM2-AS1)
NR_125797.1:n.191-3314_191-3312del (ZFPM2-AS1)
XM_011516946.1:c.1714_1716del (ZFPM2)	XP_011515248.1:p.Asn572del
XM_011516947.1:c.1645_1647del (ZFPM2)	XP_011515249.1:p.Asn549del
XM_011516948.1:c.1516_1518del (ZFPM2)	XP_011515250.1:p.Asn506del
XM_011516949.1:c.1507_1509del (ZFPM2)	XP_011515251.1:p.Asn503del
NM_001362836.1:c.1516_1518del (ZFPM2)	NP_001349765.1:p.Asn506del
NM_001362837.1:c.1279_1281del (ZFPM2)	NP_001349766.1:p.Asn427del
XM_011516947.3:c.1645_1647del (ZFPM2)	XP_011515249.1:p.Asn549del
NM_012082.4:c.1675_1677del (ZFPM2) MANE Select	NP_036214.2:p.Asn559del
NM_001362836.2:c.1516_1518del (ZFPM2)	NP_001349765.1:p.Asn506del
NM_001362837.2:c.1279_1281del (ZFPM2)	NP_001349766.1:p.Asn427del