Canonical Allele Identifier: CA371951676

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• COSMIC: COSM4759866
• MyVariant Identifiers: chr8:g.106813974T>C (hg19) ; chr8:g.105801746T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801746T>C , CM000670.2:g.105801746T>C	GRCh38
NC_000008.10:g.106813974T>C , CM000670.1:g.106813974T>C	GRCh37
NC_000008.9:g.106883150T>C	NCBI36
NG_011723.1:g.487828T>C
NG_011723.2:g.487828T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1664T>C (ZFPM2) MANE Select	ENSP00000384179.2:p.Ile555Thr
ENST00000407775.6:c.1664T>C (ZFPM2)	ENSP00000384179.2:p.Ile555Thr
ENST00000517361.1:c.1268T>C (ZFPM2)	ENSP00000428720.1:p.Ile423Thr
ENST00000520492.5:c.1268T>C (ZFPM2)	ENSP00000430757.1:p.Ile423Thr
ENST00000522296.1:n.1458T>C (ZFPM2)
NM_012082.3:c.1664T>C (ZFPM2)	NP_036214.2:p.Ile555Thr
NR_125796.1:n.180-3304A>G (ZFPM2-AS1)
NR_125797.1:n.191-3304A>G (ZFPM2-AS1)
XM_011516946.1:c.1703T>C (ZFPM2)	XP_011515248.1:p.Ile568Thr
XM_011516947.1:c.1634T>C (ZFPM2)	XP_011515249.1:p.Ile545Thr
XM_011516948.1:c.1505T>C (ZFPM2)	XP_011515250.1:p.Ile502Thr
XM_011516949.1:c.1496T>C (ZFPM2)	XP_011515251.1:p.Ile499Thr
NM_001362836.1:c.1505T>C (ZFPM2)	NP_001349765.1:p.Ile502Thr
NM_001362837.1:c.1268T>C (ZFPM2)	NP_001349766.1:p.Ile423Thr
XM_011516947.3:c.1634T>C (ZFPM2)	XP_011515249.1:p.Ile545Thr
NM_012082.4:c.1664T>C (ZFPM2) MANE Select	NP_036214.2:p.Ile555Thr
NM_001362836.2:c.1505T>C (ZFPM2)	NP_001349765.1:p.Ile502Thr
NM_001362837.2:c.1268T>C (ZFPM2)	NP_001349766.1:p.Ile423Thr