Canonical Allele Identifier: CA1618398834

Gene: ZFP57

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672656G= , CM000668.2:g.29672656G=	GRCh38
NC_000006.11:g.29640433G= , CM000668.1:g.29640433G=	GRCh37
NC_000006.10:g.29748412G=	NCBI36
NG_013045.1:g.9499C=
NG_031873.1:g.20676G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376883.2:c.1455C= MANE Select	ENSP00000366080.2:p.Phe485=
ENST00000488757.6:c.1239C=	ENSP00000418259.2:p.Phe413=
ENST00000376881.4:c.1203C=	ENSP00000366078.4:p.Phe401=
ENST00000376883.1:c.1395C=	ENSP00000366080.1:p.Phe465=
ENST00000488757.5:c.1455C=	ENSP00000418259.1:p.Phe485=
NM_001109809.2:c.1455C=	NP_001103279.2:p.Phe485=
XM_006715087.2:c.1239C=	XP_006715150.1:p.Phe413=
XM_011514570.1:c.1455C=	XP_011512872.1:p.Phe485=
NM_001109809.3:c.1455C=	NP_001103279.2:p.Phe485=
NM_001366333.1:c.1239C=	NP_001353262.1:p.Phe413=
NM_001109809.4:c.1455C=	NP_001103279.2:p.Phe485=
NM_001366333.2:c.1239C=	NP_001353262.1:p.Phe413=
NM_001109809.5:c.1455C= MANE Select	NP_001103279.2:p.Phe485=