Canonical Allele Identifier: CA371951058

Gene: ZFPM2 ZFPM2-AS1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1552G>C (ZFPM2) MANE Select	ENSP00000384179.2:p.Ala518Pro
ENST00000407775.6:c.1552G>C (ZFPM2)	ENSP00000384179.2:p.Ala518Pro
ENST00000517361.1:c.1156G>C (ZFPM2)	ENSP00000428720.1:p.Ala386Pro
ENST00000520492.5:c.1156G>C (ZFPM2)	ENSP00000430757.1:p.Ala386Pro
ENST00000522296.1:n.1346G>C (ZFPM2)
NM_012082.3:c.1552G>C (ZFPM2)	NP_036214.2:p.Ala518Pro
NR_125796.1:n.180-3192C>G (ZFPM2-AS1)
NR_125797.1:n.191-3192C>G (ZFPM2-AS1)
XM_011516946.1:c.1591G>C (ZFPM2)	XP_011515248.1:p.Ala531Pro
XM_011516947.1:c.1522G>C (ZFPM2)	XP_011515249.1:p.Ala508Pro
XM_011516948.1:c.1393G>C (ZFPM2)	XP_011515250.1:p.Ala465Pro
XM_011516949.1:c.1384G>C (ZFPM2)	XP_011515251.1:p.Ala462Pro
NM_001362836.1:c.1393G>C (ZFPM2)	NP_001349765.1:p.Ala465Pro
NM_001362837.1:c.1156G>C (ZFPM2)	NP_001349766.1:p.Ala386Pro
XM_011516947.3:c.1522G>C (ZFPM2)	XP_011515249.1:p.Ala508Pro
NM_012082.4:c.1552G>C (ZFPM2) MANE Select	NP_036214.2:p.Ala518Pro
NM_001362836.2:c.1393G>C (ZFPM2)	NP_001349765.1:p.Ala465Pro
NM_001362837.2:c.1156G>C (ZFPM2)	NP_001349766.1:p.Ala386Pro