Canonical Allele Identifier: CA363043134

Gene: ZFP57

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376883.2:c.1459C>A MANE Select	ENSP00000366080.2:p.His487Asn
ENST00000488757.6:c.1243C>A	ENSP00000418259.2:p.His415Asn
ENST00000376881.4:c.1207C>A	ENSP00000366078.4:p.His403Asn
ENST00000376883.1:c.1399C>A	ENSP00000366080.1:p.His467Asn
ENST00000488757.5:c.1459C>A	ENSP00000418259.1:p.His487Asn
NM_001109809.2:c.1459C>A	NP_001103279.2:p.His487Asn
XM_006715087.2:c.1243C>A	XP_006715150.1:p.His415Asn
XM_011514570.1:c.1459C>A	XP_011512872.1:p.His487Asn
NM_001109809.3:c.1459C>A	NP_001103279.2:p.His487Asn
NM_001366333.1:c.1243C>A	NP_001353262.1:p.His415Asn
NM_001109809.4:c.1459C>A	NP_001103279.2:p.His487Asn
NM_001366333.2:c.1243C>A	NP_001353262.1:p.His415Asn
NM_001109809.5:c.1459C>A MANE Select	NP_001103279.2:p.His487Asn