Canonical Allele Identifier: CA371950980

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• COSMIC: COSM3643753
• MyVariant Identifiers: chr8:g.106813839T>A (hg19) ; chr8:g.105801611T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801611T>A , CM000670.2:g.105801611T>A	GRCh38
NC_000008.10:g.106813839T>A , CM000670.1:g.106813839T>A	GRCh37
NC_000008.9:g.106883015T>A	NCBI36
NG_011723.1:g.487693T>A
NG_011723.2:g.487693T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1529T>A (ZFPM2) MANE Select	ENSP00000384179.2:p.Val510Asp
ENST00000407775.6:c.1529T>A (ZFPM2)	ENSP00000384179.2:p.Val510Asp
ENST00000517361.1:c.1133T>A (ZFPM2)	ENSP00000428720.1:p.Val378Asp
ENST00000520492.5:c.1133T>A (ZFPM2)	ENSP00000430757.1:p.Val378Asp
ENST00000522296.1:n.1323T>A (ZFPM2)
NM_012082.3:c.1529T>A (ZFPM2)	NP_036214.2:p.Val510Asp
NR_125796.1:n.180-3169A>T (ZFPM2-AS1)
NR_125797.1:n.191-3169A>T (ZFPM2-AS1)
XM_011516946.1:c.1568T>A (ZFPM2)	XP_011515248.1:p.Val523Asp
XM_011516947.1:c.1499T>A (ZFPM2)	XP_011515249.1:p.Val500Asp
XM_011516948.1:c.1370T>A (ZFPM2)	XP_011515250.1:p.Val457Asp
XM_011516949.1:c.1361T>A (ZFPM2)	XP_011515251.1:p.Val454Asp
NM_001362836.1:c.1370T>A (ZFPM2)	NP_001349765.1:p.Val457Asp
NM_001362837.1:c.1133T>A (ZFPM2)	NP_001349766.1:p.Val378Asp
XM_011516947.3:c.1499T>A (ZFPM2)	XP_011515249.1:p.Val500Asp
NM_012082.4:c.1529T>A (ZFPM2) MANE Select	NP_036214.2:p.Val510Asp
NM_001362836.2:c.1370T>A (ZFPM2)	NP_001349765.1:p.Val457Asp
NM_001362837.2:c.1133T>A (ZFPM2)	NP_001349766.1:p.Val378Asp