Canonical Allele Identifier: CA363043170

Gene: ZFP57

Linked Data

• gnomAD v4: 6-29672666-C-A
• MyVariant Identifiers: chr6:g.29640443C>A (hg19) ; chr6:g.29672666C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672666C>A , CM000668.2:g.29672666C>A	GRCh38
NC_000006.11:g.29640443C>A , CM000668.1:g.29640443C>A	GRCh37
NC_000006.10:g.29748422C>A	NCBI36
NG_013045.1:g.9489G>T
NG_031873.1:g.20686C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376883.2:c.1445G>T MANE Select	ENSP00000366080.2:p.Trp482Leu
ENST00000488757.6:c.1229G>T	ENSP00000418259.2:p.Trp410Leu
ENST00000376881.4:c.1193G>T	ENSP00000366078.4:p.Trp398Leu
ENST00000376883.1:c.1385G>T	ENSP00000366080.1:p.Trp462Leu
ENST00000488757.5:c.1445G>T	ENSP00000418259.1:p.Trp482Leu
NM_001109809.2:c.1445G>T	NP_001103279.2:p.Trp482Leu
XM_006715087.2:c.1229G>T	XP_006715150.1:p.Trp410Leu
XM_011514570.1:c.1445G>T	XP_011512872.1:p.Trp482Leu
NM_001109809.3:c.1445G>T	NP_001103279.2:p.Trp482Leu
NM_001366333.1:c.1229G>T	NP_001353262.1:p.Trp410Leu
NM_001109809.4:c.1445G>T	NP_001103279.2:p.Trp482Leu
NM_001366333.2:c.1229G>T	NP_001353262.1:p.Trp410Leu
NM_001109809.5:c.1445G>T MANE Select	NP_001103279.2:p.Trp482Leu