Canonical Allele Identifier: CA363043414

Gene: ZFP57

Linked Data

• MyVariant Identifiers: chr6:g.29640542A>T (hg19) ; chr6:g.29672765A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672765A>T , CM000668.2:g.29672765A>T	GRCh38
NC_000006.11:g.29640542A>T , CM000668.1:g.29640542A>T	GRCh37
NC_000006.10:g.29748521A>T	NCBI36
NG_013045.1:g.9390T>A
NG_031873.1:g.20785A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376883.2:c.1346T>A MANE Select	ENSP00000366080.2:p.Phe449Tyr
ENST00000488757.6:c.1130T>A	ENSP00000418259.2:p.Phe377Tyr
ENST00000376881.4:c.1094T>A	ENSP00000366078.4:p.Phe365Tyr
ENST00000376883.1:c.1286T>A	ENSP00000366080.1:p.Phe429Tyr
ENST00000488757.5:c.1346T>A	ENSP00000418259.1:p.Phe449Tyr
NM_001109809.2:c.1346T>A	NP_001103279.2:p.Phe449Tyr
XM_006715087.2:c.1130T>A	XP_006715150.1:p.Phe377Tyr
XM_011514570.1:c.1346T>A	XP_011512872.1:p.Phe449Tyr
NM_001109809.3:c.1346T>A	NP_001103279.2:p.Phe449Tyr
NM_001366333.1:c.1130T>A	NP_001353262.1:p.Phe377Tyr
NM_001109809.4:c.1346T>A	NP_001103279.2:p.Phe449Tyr
NM_001366333.2:c.1130T>A	NP_001353262.1:p.Phe377Tyr
NM_001109809.5:c.1346T>A MANE Select	NP_001103279.2:p.Phe449Tyr