Canonical Allele Identifier: CA1618398866
Gene: ZFP57 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29672750C= , CM000668.2:g.29672750C= GRCh38
NC_000006.11:g.29640527C= , CM000668.1:g.29640527C= GRCh37
NC_000006.10:g.29748506C= NCBI36
NG_013045.1:g.9405G=
NG_031873.1:g.20770C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376883.2:c.1361G= MANE Select ENSP00000366080.2:p.Gly454=
ENST00000488757.6:c.1145G= ENSP00000418259.2:p.Gly382=
ENST00000376881.4:c.1109G= ENSP00000366078.4:p.Gly370=
ENST00000376883.1:c.1301G= ENSP00000366080.1:p.Gly434=
ENST00000488757.5:c.1361G= ENSP00000418259.1:p.Gly454=
NM_001109809.2:c.1361G= NP_001103279.2:p.Gly454=
XM_006715087.2:c.1145G= XP_006715150.1:p.Gly382=
XM_011514570.1:c.1361G= XP_011512872.1:p.Gly454=
NM_001109809.3:c.1361G= NP_001103279.2:p.Gly454=
NM_001366333.1:c.1145G= NP_001353262.1:p.Gly382=
NM_001109809.4:c.1361G= NP_001103279.2:p.Gly454=
NM_001366333.2:c.1145G= NP_001353262.1:p.Gly382=
NM_001109809.5:c.1361G= MANE Select NP_001103279.2:p.Gly454=