Canonical Allele Identifier: CA371950968

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• COSMIC: COSM3884577
• MyVariant Identifiers: chr8:g.106813836T>C (hg19) ; chr8:g.105801608T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801608T>C , CM000670.2:g.105801608T>C	GRCh38
NC_000008.10:g.106813836T>C , CM000670.1:g.106813836T>C	GRCh37
NC_000008.9:g.106883012T>C	NCBI36
NG_011723.1:g.487690T>C
NG_011723.2:g.487690T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1526T>C (ZFPM2) MANE Select	ENSP00000384179.2:p.Met509Thr
ENST00000407775.6:c.1526T>C (ZFPM2)	ENSP00000384179.2:p.Met509Thr
ENST00000517361.1:c.1130T>C (ZFPM2)	ENSP00000428720.1:p.Met377Thr
ENST00000520492.5:c.1130T>C (ZFPM2)	ENSP00000430757.1:p.Met377Thr
ENST00000522296.1:n.1320T>C (ZFPM2)
NM_012082.3:c.1526T>C (ZFPM2)	NP_036214.2:p.Met509Thr
NR_125796.1:n.180-3166A>G (ZFPM2-AS1)
NR_125797.1:n.191-3166A>G (ZFPM2-AS1)
XM_011516946.1:c.1565T>C (ZFPM2)	XP_011515248.1:p.Met522Thr
XM_011516947.1:c.1496T>C (ZFPM2)	XP_011515249.1:p.Met499Thr
XM_011516948.1:c.1367T>C (ZFPM2)	XP_011515250.1:p.Met456Thr
XM_011516949.1:c.1358T>C (ZFPM2)	XP_011515251.1:p.Met453Thr
NM_001362836.1:c.1367T>C (ZFPM2)	NP_001349765.1:p.Met456Thr
NM_001362837.1:c.1130T>C (ZFPM2)	NP_001349766.1:p.Met377Thr
XM_011516947.3:c.1496T>C (ZFPM2)	XP_011515249.1:p.Met499Thr
NM_012082.4:c.1526T>C (ZFPM2) MANE Select	NP_036214.2:p.Met509Thr
NM_001362836.2:c.1367T>C (ZFPM2)	NP_001349765.1:p.Met456Thr
NM_001362837.2:c.1130T>C (ZFPM2)	NP_001349766.1:p.Met377Thr