Canonical Allele Identifier: CA1618398843
Gene: ZFP57 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29672682C= , CM000668.2:g.29672682C= GRCh38
NC_000006.11:g.29640459C= , CM000668.1:g.29640459C= GRCh37
NC_000006.10:g.29748438C= NCBI36
NG_013045.1:g.9473G=
NG_031873.1:g.20702C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376883.2:c.1429G= MANE Select ENSP00000366080.2:p.Val477=
ENST00000488757.6:c.1213G= ENSP00000418259.2:p.Val405=
ENST00000376881.4:c.1177G= ENSP00000366078.4:p.Val393=
ENST00000376883.1:c.1369G= ENSP00000366080.1:p.Val457=
ENST00000488757.5:c.1429G= ENSP00000418259.1:p.Val477=
NM_001109809.2:c.1429G= NP_001103279.2:p.Val477=
XM_006715087.2:c.1213G= XP_006715150.1:p.Val405=
XM_011514570.1:c.1429G= XP_011512872.1:p.Val477=
NM_001109809.3:c.1429G= NP_001103279.2:p.Val477=
NM_001366333.1:c.1213G= NP_001353262.1:p.Val405=
NM_001109809.4:c.1429G= NP_001103279.2:p.Val477=
NM_001366333.2:c.1213G= NP_001353262.1:p.Val405=
NM_001109809.5:c.1429G= MANE Select NP_001103279.2:p.Val477=