Canonical Allele Identifier: CA449458329

Gene: ZFP57

Linked Data

• MyVariant Identifiers: chr6:g.29640427A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672650A>G , CM000668.2:g.29672650A>G	GRCh38
NC_000006.11:g.29640427A>G , CM000668.1:g.29640427A>G	GRCh37
NC_000006.10:g.29748406A>G	NCBI36
NG_013045.1:g.9505T>C
NG_031873.1:g.20670A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376883.2:c.1461T>C MANE Select	ENSP00000366080.2:p.His487=
ENST00000488757.6:c.1245T>C	ENSP00000418259.2:p.His415=
ENST00000376881.4:c.1209T>C	ENSP00000366078.4:p.His403=
ENST00000376883.1:c.1401T>C	ENSP00000366080.1:p.His467=
ENST00000488757.5:c.1461T>C	ENSP00000418259.1:p.His487=
NM_001109809.2:c.1461T>C	NP_001103279.2:p.His487=
XM_006715087.2:c.1245T>C	XP_006715150.1:p.His415=
XM_011514570.1:c.1461T>C	XP_011512872.1:p.His487=
NM_001109809.3:c.1461T>C	NP_001103279.2:p.His487=
NM_001366333.1:c.1245T>C	NP_001353262.1:p.His415=
NM_001109809.4:c.1461T>C	NP_001103279.2:p.His487=
NM_001366333.2:c.1245T>C	NP_001353262.1:p.His415=
NM_001109809.5:c.1461T>C MANE Select	NP_001103279.2:p.His487=