Canonical Allele Identifier: CA371950947

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• ClinVar Variation Id: 450054
• ClinVar RCV Id: RCV000522745
• dbSNP Id: rs1194484043
• gnomAD v2: 8-106813830-T-C
• gnomAD v3: 8-105801602-T-C
• gnomAD v4: 8-105801602-T-C
• MyVariant Identifiers: chr8:g.106813830T>C (hg19) ; chr8:g.105801602T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801602T>C , CM000670.2:g.105801602T>C	GRCh38
NC_000008.10:g.106813830T>C , CM000670.1:g.106813830T>C	GRCh37
NC_000008.9:g.106883006T>C	NCBI36
NG_011723.1:g.487684T>C
NG_011723.2:g.487684T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1520T>C (ZFPM2) MANE Select	ENSP00000384179.2:p.Ile507Thr
ENST00000407775.6:c.1520T>C (ZFPM2)	ENSP00000384179.2:p.Ile507Thr
ENST00000517361.1:c.1124T>C (ZFPM2)	ENSP00000428720.1:p.Ile375Thr
ENST00000520492.5:c.1124T>C (ZFPM2)	ENSP00000430757.1:p.Ile375Thr
ENST00000522296.1:n.1314T>C (ZFPM2)
NM_012082.3:c.1520T>C (ZFPM2)	NP_036214.2:p.Ile507Thr
NR_125796.1:n.180-3160A>G (ZFPM2-AS1)
NR_125797.1:n.191-3160A>G (ZFPM2-AS1)
XM_011516946.1:c.1559T>C (ZFPM2)	XP_011515248.1:p.Ile520Thr
XM_011516947.1:c.1490T>C (ZFPM2)	XP_011515249.1:p.Ile497Thr
XM_011516948.1:c.1361T>C (ZFPM2)	XP_011515250.1:p.Ile454Thr
XM_011516949.1:c.1352T>C (ZFPM2)	XP_011515251.1:p.Ile451Thr
NM_001362836.1:c.1361T>C (ZFPM2)	NP_001349765.1:p.Ile454Thr
NM_001362837.1:c.1124T>C (ZFPM2)	NP_001349766.1:p.Ile375Thr
XM_011516947.3:c.1490T>C (ZFPM2)	XP_011515249.1:p.Ile497Thr
NM_012082.4:c.1520T>C (ZFPM2) MANE Select	NP_036214.2:p.Ile507Thr
NM_001362836.2:c.1361T>C (ZFPM2)	NP_001349765.1:p.Ile454Thr
NM_001362837.2:c.1124T>C (ZFPM2)	NP_001349766.1:p.Ile375Thr