Canonical Allele Identifier: CA371951059

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• MyVariant Identifiers: chr8:g.106813862G>T (hg19) ; chr8:g.105801634G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801634G>T , CM000670.2:g.105801634G>T	GRCh38
NC_000008.10:g.106813862G>T , CM000670.1:g.106813862G>T	GRCh37
NC_000008.9:g.106883038G>T	NCBI36
NG_011723.1:g.487716G>T
NG_011723.2:g.487716G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1552G>T (ZFPM2) MANE Select	ENSP00000384179.2:p.Ala518Ser
ENST00000407775.6:c.1552G>T (ZFPM2)	ENSP00000384179.2:p.Ala518Ser
ENST00000517361.1:c.1156G>T (ZFPM2)	ENSP00000428720.1:p.Ala386Ser
ENST00000520492.5:c.1156G>T (ZFPM2)	ENSP00000430757.1:p.Ala386Ser
ENST00000522296.1:n.1346G>T (ZFPM2)
NM_012082.3:c.1552G>T (ZFPM2)	NP_036214.2:p.Ala518Ser
NR_125796.1:n.180-3192C>A (ZFPM2-AS1)
NR_125797.1:n.191-3192C>A (ZFPM2-AS1)
XM_011516946.1:c.1591G>T (ZFPM2)	XP_011515248.1:p.Ala531Ser
XM_011516947.1:c.1522G>T (ZFPM2)	XP_011515249.1:p.Ala508Ser
XM_011516948.1:c.1393G>T (ZFPM2)	XP_011515250.1:p.Ala465Ser
XM_011516949.1:c.1384G>T (ZFPM2)	XP_011515251.1:p.Ala462Ser
NM_001362836.1:c.1393G>T (ZFPM2)	NP_001349765.1:p.Ala465Ser
NM_001362837.1:c.1156G>T (ZFPM2)	NP_001349766.1:p.Ala386Ser
XM_011516947.3:c.1522G>T (ZFPM2)	XP_011515249.1:p.Ala508Ser
NM_012082.4:c.1552G>T (ZFPM2) MANE Select	NP_036214.2:p.Ala518Ser
NM_001362836.2:c.1393G>T (ZFPM2)	NP_001349765.1:p.Ala465Ser
NM_001362837.2:c.1156G>T (ZFPM2)	NP_001349766.1:p.Ala386Ser