Canonical Allele Identifier: CA371950863

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• MyVariant Identifiers: chr8:g.106813811T>A (hg19) ; chr8:g.105801583T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801583T>A , CM000670.2:g.105801583T>A	GRCh38
NC_000008.10:g.106813811T>A , CM000670.1:g.106813811T>A	GRCh37
NC_000008.9:g.106882987T>A	NCBI36
NG_011723.1:g.487665T>A
NG_011723.2:g.487665T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1501T>A (ZFPM2) MANE Select	ENSP00000384179.2:p.Phe501Ile
ENST00000407775.6:c.1501T>A (ZFPM2)	ENSP00000384179.2:p.Phe501Ile
ENST00000517361.1:c.1105T>A (ZFPM2)	ENSP00000428720.1:p.Phe369Ile
ENST00000520492.5:c.1105T>A (ZFPM2)	ENSP00000430757.1:p.Phe369Ile
ENST00000522296.1:n.1295T>A (ZFPM2)
NM_012082.3:c.1501T>A (ZFPM2)	NP_036214.2:p.Phe501Ile
NR_125796.1:n.180-3141A>T (ZFPM2-AS1)
NR_125797.1:n.191-3141A>T (ZFPM2-AS1)
XM_011516946.1:c.1540T>A (ZFPM2)	XP_011515248.1:p.Phe514Ile
XM_011516947.1:c.1471T>A (ZFPM2)	XP_011515249.1:p.Phe491Ile
XM_011516948.1:c.1342T>A (ZFPM2)	XP_011515250.1:p.Phe448Ile
XM_011516949.1:c.1333T>A (ZFPM2)	XP_011515251.1:p.Phe445Ile
NM_001362836.1:c.1342T>A (ZFPM2)	NP_001349765.1:p.Phe448Ile
NM_001362837.1:c.1105T>A (ZFPM2)	NP_001349766.1:p.Phe369Ile
XM_011516947.3:c.1471T>A (ZFPM2)	XP_011515249.1:p.Phe491Ile
NM_012082.4:c.1501T>A (ZFPM2) MANE Select	NP_036214.2:p.Phe501Ile
NM_001362836.2:c.1342T>A (ZFPM2)	NP_001349765.1:p.Phe448Ile
NM_001362837.2:c.1105T>A (ZFPM2)	NP_001349766.1:p.Phe369Ile