Canonical Allele Identifier: CA363043405
Gene: ZFP57 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29672762C>A , CM000668.2:g.29672762C>A GRCh38
NC_000006.11:g.29640539C>A , CM000668.1:g.29640539C>A GRCh37
NC_000006.10:g.29748518C>A NCBI36
NG_013045.1:g.9393G>T
NG_031873.1:g.20782C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376883.2:c.1349G>T MANE Select ENSP00000366080.2:p.Gly450Val
ENST00000488757.6:c.1133G>T ENSP00000418259.2:p.Gly378Val
ENST00000376881.4:c.1097G>T ENSP00000366078.4:p.Gly366Val
ENST00000376883.1:c.1289G>T ENSP00000366080.1:p.Gly430Val
ENST00000488757.5:c.1349G>T ENSP00000418259.1:p.Gly450Val
NM_001109809.2:c.1349G>T NP_001103279.2:p.Gly450Val
XM_006715087.2:c.1133G>T XP_006715150.1:p.Gly378Val
XM_011514570.1:c.1349G>T XP_011512872.1:p.Gly450Val
NM_001109809.3:c.1349G>T NP_001103279.2:p.Gly450Val
NM_001366333.1:c.1133G>T NP_001353262.1:p.Gly378Val
NM_001109809.4:c.1349G>T NP_001103279.2:p.Gly450Val
NM_001366333.2:c.1133G>T NP_001353262.1:p.Gly378Val
NM_001109809.5:c.1349G>T MANE Select NP_001103279.2:p.Gly450Val