Canonical Allele Identifier: CA371951896

Gene: ZFPM2 ZFPM2-AS1

Linked Data

• gnomAD v4: 8-105801776-T-C
• MyVariant Identifiers: chr8:g.106814004T>C (hg19) ; chr8:g.105801776T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.105801776T>C , CM000670.2:g.105801776T>C	GRCh38
NC_000008.10:g.106814004T>C , CM000670.1:g.106814004T>C	GRCh37
NC_000008.9:g.106883180T>C	NCBI36
NG_011723.1:g.487858T>C
NG_011723.2:g.487858T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407775.7:c.1694T>C (ZFPM2) MANE Select	ENSP00000384179.2:p.Val565Ala
ENST00000407775.6:c.1694T>C (ZFPM2)	ENSP00000384179.2:p.Val565Ala
ENST00000517361.1:c.1298T>C (ZFPM2)	ENSP00000428720.1:p.Val433Ala
ENST00000520492.5:c.1298T>C (ZFPM2)	ENSP00000430757.1:p.Val433Ala
ENST00000522296.1:n.1488T>C (ZFPM2)
NM_012082.3:c.1694T>C (ZFPM2)	NP_036214.2:p.Val565Ala
NR_125796.1:n.180-3334A>G (ZFPM2-AS1)
NR_125797.1:n.191-3334A>G (ZFPM2-AS1)
XM_011516946.1:c.1733T>C (ZFPM2)	XP_011515248.1:p.Val578Ala
XM_011516947.1:c.1664T>C (ZFPM2)	XP_011515249.1:p.Val555Ala
XM_011516948.1:c.1535T>C (ZFPM2)	XP_011515250.1:p.Val512Ala
XM_011516949.1:c.1526T>C (ZFPM2)	XP_011515251.1:p.Val509Ala
NM_001362836.1:c.1535T>C (ZFPM2)	NP_001349765.1:p.Val512Ala
NM_001362837.1:c.1298T>C (ZFPM2)	NP_001349766.1:p.Val433Ala
XM_011516947.3:c.1664T>C (ZFPM2)	XP_011515249.1:p.Val555Ala
NM_012082.4:c.1694T>C (ZFPM2) MANE Select	NP_036214.2:p.Val565Ala
NM_001362836.2:c.1535T>C (ZFPM2)	NP_001349765.1:p.Val512Ala
NM_001362837.2:c.1298T>C (ZFPM2)	NP_001349766.1:p.Val433Ala