Canonical Allele Identifier: CA371951128

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• dbSNP Id: rs1563573477
• gnomAD v4: 8-105801658-C-T
• COSMIC: COSM1094684
• MyVariant Identifiers: chr8:g.106813886C>T (hg19) ; chr8:g.105801658C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801658C>T , CM000670.2:g.105801658C>T	GRCh38
NC_000008.10:g.106813886C>T , CM000670.1:g.106813886C>T	GRCh37
NC_000008.9:g.106883062C>T	NCBI36
NG_011723.1:g.487740C>T
NG_011723.2:g.487740C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1576C>T (ZFPM2) MANE Select	ENSP00000384179.2:p.Arg526Trp
ENST00000407775.6:c.1576C>T (ZFPM2)	ENSP00000384179.2:p.Arg526Trp
ENST00000517361.1:c.1180C>T (ZFPM2)	ENSP00000428720.1:p.Arg394Trp
ENST00000520492.5:c.1180C>T (ZFPM2)	ENSP00000430757.1:p.Arg394Trp
ENST00000522296.1:n.1370C>T (ZFPM2)
NM_012082.3:c.1576C>T (ZFPM2)	NP_036214.2:p.Arg526Trp
NR_125796.1:n.180-3216G>A (ZFPM2-AS1)
NR_125797.1:n.191-3216G>A (ZFPM2-AS1)
XM_011516946.1:c.1615C>T (ZFPM2)	XP_011515248.1:p.Arg539Trp
XM_011516947.1:c.1546C>T (ZFPM2)	XP_011515249.1:p.Arg516Trp
XM_011516948.1:c.1417C>T (ZFPM2)	XP_011515250.1:p.Arg473Trp
XM_011516949.1:c.1408C>T (ZFPM2)	XP_011515251.1:p.Arg470Trp
NM_001362836.1:c.1417C>T (ZFPM2)	NP_001349765.1:p.Arg473Trp
NM_001362837.1:c.1180C>T (ZFPM2)	NP_001349766.1:p.Arg394Trp
XM_011516947.3:c.1546C>T (ZFPM2)	XP_011515249.1:p.Arg516Trp
NM_012082.4:c.1576C>T (ZFPM2) MANE Select	NP_036214.2:p.Arg526Trp
NM_001362836.2:c.1417C>T (ZFPM2)	NP_001349765.1:p.Arg473Trp
NM_001362837.2:c.1180C>T (ZFPM2)	NP_001349766.1:p.Arg394Trp