Canonical Allele Identifier: CA363043153

Gene: ZFP57

Linked Data

• gnomAD v4: 6-29672658-A-C
• MyVariant Identifiers: chr6:g.29640435A>C (hg19) ; chr6:g.29672658A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672658A>C , CM000668.2:g.29672658A>C	GRCh38
NC_000006.11:g.29640435A>C , CM000668.1:g.29640435A>C	GRCh37
NC_000006.10:g.29748414A>C	NCBI36
NG_013045.1:g.9497T>G
NG_031873.1:g.20678A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376883.2:c.1453T>G MANE Select	ENSP00000366080.2:p.Phe485Val
ENST00000488757.6:c.1237T>G	ENSP00000418259.2:p.Phe413Val
ENST00000376881.4:c.1201T>G	ENSP00000366078.4:p.Phe401Val
ENST00000376883.1:c.1393T>G	ENSP00000366080.1:p.Phe465Val
ENST00000488757.5:c.1453T>G	ENSP00000418259.1:p.Phe485Val
NM_001109809.2:c.1453T>G	NP_001103279.2:p.Phe485Val
XM_006715087.2:c.1237T>G	XP_006715150.1:p.Phe413Val
XM_011514570.1:c.1453T>G	XP_011512872.1:p.Phe485Val
NM_001109809.3:c.1453T>G	NP_001103279.2:p.Phe485Val
NM_001366333.1:c.1237T>G	NP_001353262.1:p.Phe413Val
NM_001109809.4:c.1453T>G	NP_001103279.2:p.Phe485Val
NM_001366333.2:c.1237T>G	NP_001353262.1:p.Phe413Val
NM_001109809.5:c.1453T>G MANE Select	NP_001103279.2:p.Phe485Val