Canonical Allele Identifier: CA363043175

Gene: ZFP57

Linked Data

• MyVariant Identifiers: chr6:g.29640444A>G (hg19) ; chr6:g.29672667A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672667A>G , CM000668.2:g.29672667A>G	GRCh38
NC_000006.11:g.29640444A>G , CM000668.1:g.29640444A>G	GRCh37
NC_000006.10:g.29748423A>G	NCBI36
NG_013045.1:g.9488T>C
NG_031873.1:g.20687A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376883.2:c.1444T>C MANE Select	ENSP00000366080.2:p.Trp482Arg
ENST00000488757.6:c.1228T>C	ENSP00000418259.2:p.Trp410Arg
ENST00000376881.4:c.1192T>C	ENSP00000366078.4:p.Trp398Arg
ENST00000376883.1:c.1384T>C	ENSP00000366080.1:p.Trp462Arg
ENST00000488757.5:c.1444T>C	ENSP00000418259.1:p.Trp482Arg
NM_001109809.2:c.1444T>C	NP_001103279.2:p.Trp482Arg
XM_006715087.2:c.1228T>C	XP_006715150.1:p.Trp410Arg
XM_011514570.1:c.1444T>C	XP_011512872.1:p.Trp482Arg
NM_001109809.3:c.1444T>C	NP_001103279.2:p.Trp482Arg
NM_001366333.1:c.1228T>C	NP_001353262.1:p.Trp410Arg
NM_001109809.4:c.1444T>C	NP_001103279.2:p.Trp482Arg
NM_001366333.2:c.1228T>C	NP_001353262.1:p.Trp410Arg
NM_001109809.5:c.1444T>C MANE Select	NP_001103279.2:p.Trp482Arg