Canonical Allele Identifier: CA371951670

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 1701554
• ClinVar RCV Id: RCV002276189
• dbSNP Id: rs781100381
• MyVariant Identifiers: chr8:g.106813973A>C (hg19) ; chr8:g.105801745A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801745A>C , CM000670.2:g.105801745A>C	GRCh38
NC_000008.10:g.106813973A>C , CM000670.1:g.106813973A>C	GRCh37
NC_000008.9:g.106883149A>C	NCBI36
NG_011723.1:g.487827A>C
NG_011723.2:g.487827A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1663A>C (ZFPM2) MANE Select	ENSP00000384179.2:p.Ile555Leu
ENST00000407775.6:c.1663A>C (ZFPM2)	ENSP00000384179.2:p.Ile555Leu
ENST00000517361.1:c.1267A>C (ZFPM2)	ENSP00000428720.1:p.Ile423Leu
ENST00000520492.5:c.1267A>C (ZFPM2)	ENSP00000430757.1:p.Ile423Leu
ENST00000522296.1:n.1457A>C (ZFPM2)
NM_012082.3:c.1663A>C (ZFPM2)	NP_036214.2:p.Ile555Leu
NR_125796.1:n.180-3303T>G (ZFPM2-AS1)
NR_125797.1:n.191-3303T>G (ZFPM2-AS1)
XM_011516946.1:c.1702A>C (ZFPM2)	XP_011515248.1:p.Ile568Leu
XM_011516947.1:c.1633A>C (ZFPM2)	XP_011515249.1:p.Ile545Leu
XM_011516948.1:c.1504A>C (ZFPM2)	XP_011515250.1:p.Ile502Leu
XM_011516949.1:c.1495A>C (ZFPM2)	XP_011515251.1:p.Ile499Leu
NM_001362836.1:c.1504A>C (ZFPM2)	NP_001349765.1:p.Ile502Leu
NM_001362837.1:c.1267A>C (ZFPM2)	NP_001349766.1:p.Ile423Leu
XM_011516947.3:c.1633A>C (ZFPM2)	XP_011515249.1:p.Ile545Leu
NM_012082.4:c.1663A>C (ZFPM2) MANE Select	NP_036214.2:p.Ile555Leu
NM_001362836.2:c.1504A>C (ZFPM2)	NP_001349765.1:p.Ile502Leu
NM_001362837.2:c.1267A>C (ZFPM2)	NP_001349766.1:p.Ile423Leu