Canonical Allele Identifier: CA462650165

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• MyVariant Identifiers: chr8:g.106813996T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801768T>C , CM000670.2:g.105801768T>C	GRCh38
NC_000008.10:g.106813996T>C , CM000670.1:g.106813996T>C	GRCh37
NC_000008.9:g.106883172T>C	NCBI36
NG_011723.1:g.487850T>C
NG_011723.2:g.487850T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1686T>C (ZFPM2) MANE Select	ENSP00000384179.2:p.Asn562=
ENST00000407775.6:c.1686T>C (ZFPM2)	ENSP00000384179.2:p.Asn562=
ENST00000517361.1:c.1290T>C (ZFPM2)	ENSP00000428720.1:p.Asn430=
ENST00000520492.5:c.1290T>C (ZFPM2)	ENSP00000430757.1:p.Asn430=
ENST00000522296.1:n.1480T>C (ZFPM2)
NM_012082.3:c.1686T>C (ZFPM2)	NP_036214.2:p.Asn562=
NR_125796.1:n.180-3326A>G (ZFPM2-AS1)
NR_125797.1:n.191-3326A>G (ZFPM2-AS1)
XM_011516946.1:c.1725T>C (ZFPM2)	XP_011515248.1:p.Asn575=
XM_011516947.1:c.1656T>C (ZFPM2)	XP_011515249.1:p.Asn552=
XM_011516948.1:c.1527T>C (ZFPM2)	XP_011515250.1:p.Asn509=
XM_011516949.1:c.1518T>C (ZFPM2)	XP_011515251.1:p.Asn506=
NM_001362836.1:c.1527T>C (ZFPM2)	NP_001349765.1:p.Asn509=
NM_001362837.1:c.1290T>C (ZFPM2)	NP_001349766.1:p.Asn430=
XM_011516947.3:c.1656T>C (ZFPM2)	XP_011515249.1:p.Asn552=
NM_012082.4:c.1686T>C (ZFPM2) MANE Select	NP_036214.2:p.Asn562=
NM_001362836.2:c.1527T>C (ZFPM2)	NP_001349765.1:p.Asn509=
NM_001362837.2:c.1290T>C (ZFPM2)	NP_001349766.1:p.Asn430=