Canonical Allele Identifier: CA371952562

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• gnomAD v4: 8-105801937-C-A
• MyVariant Identifiers: chr8:g.106814165C>A (hg19) ; chr8:g.105801937C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801937C>A , CM000670.2:g.105801937C>A	GRCh38
NC_000008.10:g.106814165C>A , CM000670.1:g.106814165C>A	GRCh37
NC_000008.9:g.106883341C>A	NCBI36
NG_011723.1:g.488019C>A
NG_011723.2:g.488019C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1855C>A (ZFPM2) MANE Select	ENSP00000384179.2:p.Pro619Thr
ENST00000407775.6:c.1855C>A (ZFPM2)	ENSP00000384179.2:p.Pro619Thr
ENST00000517361.1:c.1459C>A (ZFPM2)	ENSP00000428720.1:p.Pro487Thr
ENST00000520492.5:c.1459C>A (ZFPM2)	ENSP00000430757.1:p.Pro487Thr
ENST00000522296.1:n.1649C>A (ZFPM2)
NM_012082.3:c.1855C>A (ZFPM2)	NP_036214.2:p.Pro619Thr
NR_125796.1:n.180-3495G>T (ZFPM2-AS1)
NR_125797.1:n.191-3495G>T (ZFPM2-AS1)
XM_011516946.1:c.1894C>A (ZFPM2)	XP_011515248.1:p.Pro632Thr
XM_011516947.1:c.1825C>A (ZFPM2)	XP_011515249.1:p.Pro609Thr
XM_011516948.1:c.1696C>A (ZFPM2)	XP_011515250.1:p.Pro566Thr
XM_011516949.1:c.1687C>A (ZFPM2)	XP_011515251.1:p.Pro563Thr
NM_001362836.1:c.1696C>A (ZFPM2)	NP_001349765.1:p.Pro566Thr
NM_001362837.1:c.1459C>A (ZFPM2)	NP_001349766.1:p.Pro487Thr
XM_011516947.3:c.1825C>A (ZFPM2)	XP_011515249.1:p.Pro609Thr
NM_012082.4:c.1855C>A (ZFPM2) MANE Select	NP_036214.2:p.Pro619Thr
NM_001362836.2:c.1696C>A (ZFPM2)	NP_001349765.1:p.Pro566Thr
NM_001362837.2:c.1459C>A (ZFPM2)	NP_001349766.1:p.Pro487Thr