Canonical Allele Identifier: CA371951137

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 2572676
• ClinVar RCV Id: RCV003314790
• gnomAD v4: 8-105801661-C-T
• MyVariant Identifiers: chr8:g.106813889C>T (hg19) ; chr8:g.105801661C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801661C>T , CM000670.2:g.105801661C>T	GRCh38
NC_000008.10:g.106813889C>T , CM000670.1:g.106813889C>T	GRCh37
NC_000008.9:g.106883065C>T	NCBI36
NG_011723.1:g.487743C>T
NG_011723.2:g.487743C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1579C>T (ZFPM2) MANE Select	ENSP00000384179.2:p.Arg527Ter
ENST00000407775.6:c.1579C>T (ZFPM2)	ENSP00000384179.2:p.Arg527Ter
ENST00000517361.1:c.1183C>T (ZFPM2)	ENSP00000428720.1:p.Arg395Ter
ENST00000520492.5:c.1183C>T (ZFPM2)	ENSP00000430757.1:p.Arg395Ter
ENST00000522296.1:n.1373C>T (ZFPM2)
NM_012082.3:c.1579C>T (ZFPM2)	NP_036214.2:p.Arg527Ter
NR_125796.1:n.180-3219G>A (ZFPM2-AS1)
NR_125797.1:n.191-3219G>A (ZFPM2-AS1)
XM_011516946.1:c.1618C>T (ZFPM2)	XP_011515248.1:p.Arg540Ter
XM_011516947.1:c.1549C>T (ZFPM2)	XP_011515249.1:p.Arg517Ter
XM_011516948.1:c.1420C>T (ZFPM2)	XP_011515250.1:p.Arg474Ter
XM_011516949.1:c.1411C>T (ZFPM2)	XP_011515251.1:p.Arg471Ter
NM_001362836.1:c.1420C>T (ZFPM2)	NP_001349765.1:p.Arg474Ter
NM_001362837.1:c.1183C>T (ZFPM2)	NP_001349766.1:p.Arg395Ter
XM_011516947.3:c.1549C>T (ZFPM2)	XP_011515249.1:p.Arg517Ter
NM_012082.4:c.1579C>T (ZFPM2) MANE Select	NP_036214.2:p.Arg527Ter
NM_001362836.2:c.1420C>T (ZFPM2)	NP_001349765.1:p.Arg474Ter
NM_001362837.2:c.1183C>T (ZFPM2)	NP_001349766.1:p.Arg395Ter