Canonical Allele Identifier: CA449458337
Gene: ZFP57 HGNC NCBI

Linked Data

gnomAD v4: 6-29672758-C-T
MyVariant Identifiers: chr6:g.29640535C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29672758C>T , CM000668.2:g.29672758C>T GRCh38
NC_000006.11:g.29640535C>T , CM000668.1:g.29640535C>T GRCh37
NC_000006.10:g.29748514C>T NCBI36
NG_013045.1:g.9397G>A
NG_031873.1:g.20778C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376883.2:c.1353G>A MANE Select ENSP00000366080.2:p.Glu451=
ENST00000488757.6:c.1137G>A ENSP00000418259.2:p.Glu379=
ENST00000376881.4:c.1101G>A ENSP00000366078.4:p.Glu367=
ENST00000376883.1:c.1293G>A ENSP00000366080.1:p.Glu431=
ENST00000488757.5:c.1353G>A ENSP00000418259.1:p.Glu451=
NM_001109809.2:c.1353G>A NP_001103279.2:p.Glu451=
XM_006715087.2:c.1137G>A XP_006715150.1:p.Glu379=
XM_011514570.1:c.1353G>A XP_011512872.1:p.Glu451=
NM_001109809.3:c.1353G>A NP_001103279.2:p.Glu451=
NM_001366333.1:c.1137G>A NP_001353262.1:p.Glu379=
NM_001109809.4:c.1353G>A NP_001103279.2:p.Glu451=
NM_001366333.2:c.1137G>A NP_001353262.1:p.Glu379=
NM_001109809.5:c.1353G>A MANE Select NP_001103279.2:p.Glu451=