Canonical Allele Identifier: CA251577

Gene: ZFP57

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29673328G>T , CM000668.2:g.29673328G>T	GRCh38
NC_000006.11:g.29641105G>T , CM000668.1:g.29641105G>T	GRCh37
NC_000006.10:g.29749084G>T	NCBI36
NG_013045.1:g.8827C>A
NG_031873.1:g.21348G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376883.2:c.783C>A MANE Select	ENSP00000366080.2:p.Cys261Ter
ENST00000488757.6:c.567C>A	ENSP00000418259.2:p.Cys189Ter
ENST00000376881.4:c.531C>A	ENSP00000366078.4:p.Cys177Ter
ENST00000376883.1:c.723C>A	ENSP00000366080.1:p.Cys241Ter
ENST00000488757.5:c.783C>A	ENSP00000418259.1:p.Cys261Ter
NM_001109809.2:c.783C>A	NP_001103279.2:p.Cys261Ter
XM_006715087.2:c.567C>A	XP_006715150.1:p.Cys189Ter
XM_011514570.1:c.783C>A	XP_011512872.1:p.Cys261Ter
NM_001109809.3:c.783C>A	NP_001103279.2:p.Cys261Ter
NM_001366333.1:c.567C>A	NP_001353262.1:p.Cys189Ter
NM_001109809.4:c.783C>A	NP_001103279.2:p.Cys261Ter
NM_001366333.2:c.567C>A	NP_001353262.1:p.Cys189Ter
NM_001109809.5:c.783C>A MANE Select	NP_001103279.2:p.Cys261Ter