Canonical Allele Identifier: CA1618398831
Gene: ZFP57 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29672651T= , CM000668.2:g.29672651T= GRCh38
NC_000006.11:g.29640428T= , CM000668.1:g.29640428T= GRCh37
NC_000006.10:g.29748407T= NCBI36
NG_013045.1:g.9504A=
NG_031873.1:g.20671T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376883.2:c.1460A= MANE Select ENSP00000366080.2:p.His487=
ENST00000488757.6:c.1244A= ENSP00000418259.2:p.His415=
ENST00000376881.4:c.1208A= ENSP00000366078.4:p.His403=
ENST00000376883.1:c.1400A= ENSP00000366080.1:p.His467=
ENST00000488757.5:c.1460A= ENSP00000418259.1:p.His487=
NM_001109809.2:c.1460A= NP_001103279.2:p.His487=
XM_006715087.2:c.1244A= XP_006715150.1:p.His415=
XM_011514570.1:c.1460A= XP_011512872.1:p.His487=
NM_001109809.3:c.1460A= NP_001103279.2:p.His487=
NM_001366333.1:c.1244A= NP_001353262.1:p.His415=
NM_001109809.4:c.1460A= NP_001103279.2:p.His487=
NM_001366333.2:c.1244A= NP_001353262.1:p.His415=
NM_001109809.5:c.1460A= MANE Select NP_001103279.2:p.His487=