Canonical Allele Identifier: CA363043133

Gene: ZFP57

Linked Data

• MyVariant Identifiers: chr6:g.29640429G>C (hg19) ; chr6:g.29672652G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672652G>C , CM000668.2:g.29672652G>C	GRCh38
NC_000006.11:g.29640429G>C , CM000668.1:g.29640429G>C	GRCh37
NC_000006.10:g.29748408G>C	NCBI36
NG_013045.1:g.9503C>G
NG_031873.1:g.20672G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376883.2:c.1459C>G MANE Select	ENSP00000366080.2:p.His487Asp
ENST00000488757.6:c.1243C>G	ENSP00000418259.2:p.His415Asp
ENST00000376881.4:c.1207C>G	ENSP00000366078.4:p.His403Asp
ENST00000376883.1:c.1399C>G	ENSP00000366080.1:p.His467Asp
ENST00000488757.5:c.1459C>G	ENSP00000418259.1:p.His487Asp
NM_001109809.2:c.1459C>G	NP_001103279.2:p.His487Asp
XM_006715087.2:c.1243C>G	XP_006715150.1:p.His415Asp
XM_011514570.1:c.1459C>G	XP_011512872.1:p.His487Asp
NM_001109809.3:c.1459C>G	NP_001103279.2:p.His487Asp
NM_001366333.1:c.1243C>G	NP_001353262.1:p.His415Asp
NM_001109809.4:c.1459C>G	NP_001103279.2:p.His487Asp
NM_001366333.2:c.1243C>G	NP_001353262.1:p.His415Asp
NM_001109809.5:c.1459C>G MANE Select	NP_001103279.2:p.His487Asp