Canonical Allele Identifier: CA363042894
Gene: ZFP57 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29672543C>G , CM000668.2:g.29672543C>G GRCh38
NC_000006.11:g.29640320C>G , CM000668.1:g.29640320C>G GRCh37
NC_000006.10:g.29748299C>G NCBI36
NG_013045.1:g.9612G>C
NG_031873.1:g.20563C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376883.2:c.1568G>C MANE Select ENSP00000366080.2:p.Gly523Ala
ENST00000488757.6:c.1352G>C ENSP00000418259.2:p.Gly451Ala
ENST00000376881.4:c.1316G>C ENSP00000366078.4:p.Gly439Ala
ENST00000376883.1:c.1508G>C ENSP00000366080.1:p.Gly503Ala
ENST00000488757.5:c.1568G>C ENSP00000418259.1:p.Gly523Ala
NM_001109809.2:c.1568G>C NP_001103279.2:p.Gly523Ala
XM_006715087.2:c.1352G>C XP_006715150.1:p.Gly451Ala
XM_011514570.1:c.1568G>C XP_011512872.1:p.Gly523Ala
NM_001109809.3:c.1568G>C NP_001103279.2:p.Gly523Ala
NM_001366333.1:c.1352G>C NP_001353262.1:p.Gly451Ala
NM_001109809.4:c.1568G>C NP_001103279.2:p.Gly523Ala
NM_001366333.2:c.1352G>C NP_001353262.1:p.Gly451Ala
NM_001109809.5:c.1568G>C MANE Select NP_001103279.2:p.Gly523Ala