Canonical Allele Identifier: CA1618398837
Gene: ZFP57 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29672661C= , CM000668.2:g.29672661C= GRCh38
NC_000006.11:g.29640438C= , CM000668.1:g.29640438C= GRCh37
NC_000006.10:g.29748417C= NCBI36
NG_013045.1:g.9494G=
NG_031873.1:g.20681C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376883.2:c.1450G= MANE Select ENSP00000366080.2:p.Gly484=
ENST00000488757.6:c.1234G= ENSP00000418259.2:p.Gly412=
ENST00000376881.4:c.1198G= ENSP00000366078.4:p.Gly400=
ENST00000376883.1:c.1390G= ENSP00000366080.1:p.Gly464=
ENST00000488757.5:c.1450G= ENSP00000418259.1:p.Gly484=
NM_001109809.2:c.1450G= NP_001103279.2:p.Gly484=
XM_006715087.2:c.1234G= XP_006715150.1:p.Gly412=
XM_011514570.1:c.1450G= XP_011512872.1:p.Gly484=
NM_001109809.3:c.1450G= NP_001103279.2:p.Gly484=
NM_001366333.1:c.1234G= NP_001353262.1:p.Gly412=
NM_001109809.4:c.1450G= NP_001103279.2:p.Gly484=
NM_001366333.2:c.1234G= NP_001353262.1:p.Gly412=
NM_001109809.5:c.1450G= MANE Select NP_001103279.2:p.Gly484=