Canonical Allele Identifier: CA449458229

Gene: ZFP57

Linked Data

• dbSNP Id: rs1460618831
• gnomAD v2: 6-29640433-G-A
• gnomAD v4: 6-29672656-G-A
• MyVariant Identifiers: chr6:g.29640433G>A (hg19) ; chr6:g.29672656G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672656G>A , CM000668.2:g.29672656G>A	GRCh38
NC_000006.11:g.29640433G>A , CM000668.1:g.29640433G>A	GRCh37
NC_000006.10:g.29748412G>A	NCBI36
NG_013045.1:g.9499C>T
NG_031873.1:g.20676G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376883.2:c.1455C>T MANE Select	ENSP00000366080.2:p.Phe485=
ENST00000488757.6:c.1239C>T	ENSP00000418259.2:p.Phe413=
ENST00000376881.4:c.1203C>T	ENSP00000366078.4:p.Phe401=
ENST00000376883.1:c.1395C>T	ENSP00000366080.1:p.Phe465=
ENST00000488757.5:c.1455C>T	ENSP00000418259.1:p.Phe485=
NM_001109809.2:c.1455C>T	NP_001103279.2:p.Phe485=
XM_006715087.2:c.1239C>T	XP_006715150.1:p.Phe413=
XM_011514570.1:c.1455C>T	XP_011512872.1:p.Phe485=
NM_001109809.3:c.1455C>T	NP_001103279.2:p.Phe485=
NM_001366333.1:c.1239C>T	NP_001353262.1:p.Phe413=
NM_001109809.4:c.1455C>T	NP_001103279.2:p.Phe485=
NM_001366333.2:c.1239C>T	NP_001353262.1:p.Phe413=
NM_001109809.5:c.1455C>T MANE Select	NP_001103279.2:p.Phe485=