Canonical Allele Identifier: CA363043132

Gene: ZFP57

Linked Data

• MyVariant Identifiers: chr6:g.29640428T>G (hg19) ; chr6:g.29672651T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672651T>G , CM000668.2:g.29672651T>G	GRCh38
NC_000006.11:g.29640428T>G , CM000668.1:g.29640428T>G	GRCh37
NC_000006.10:g.29748407T>G	NCBI36
NG_013045.1:g.9504A>C
NG_031873.1:g.20671T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376883.2:c.1460A>C MANE Select	ENSP00000366080.2:p.His487Pro
ENST00000488757.6:c.1244A>C	ENSP00000418259.2:p.His415Pro
ENST00000376881.4:c.1208A>C	ENSP00000366078.4:p.His403Pro
ENST00000376883.1:c.1400A>C	ENSP00000366080.1:p.His467Pro
ENST00000488757.5:c.1460A>C	ENSP00000418259.1:p.His487Pro
NM_001109809.2:c.1460A>C	NP_001103279.2:p.His487Pro
XM_006715087.2:c.1244A>C	XP_006715150.1:p.His415Pro
XM_011514570.1:c.1460A>C	XP_011512872.1:p.His487Pro
NM_001109809.3:c.1460A>C	NP_001103279.2:p.His487Pro
NM_001366333.1:c.1244A>C	NP_001353262.1:p.His415Pro
NM_001109809.4:c.1460A>C	NP_001103279.2:p.His487Pro
NM_001366333.2:c.1244A>C	NP_001353262.1:p.His415Pro
NM_001109809.5:c.1460A>C MANE Select	NP_001103279.2:p.His487Pro