Canonical Allele Identifier: CA363043355

Gene: ZFP57

Linked Data

• MyVariant Identifiers: chr6:g.29640517A>T (hg19) ; chr6:g.29672740A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672740A>T , CM000668.2:g.29672740A>T	GRCh38
NC_000006.11:g.29640517A>T , CM000668.1:g.29640517A>T	GRCh37
NC_000006.10:g.29748496A>T	NCBI36
NG_013045.1:g.9415T>A
NG_031873.1:g.20760A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376883.2:c.1371T>A MANE Select	ENSP00000366080.2:p.Asp457Glu
ENST00000488757.6:c.1155T>A	ENSP00000418259.2:p.Asp385Glu
ENST00000376881.4:c.1119T>A	ENSP00000366078.4:p.Asp373Glu
ENST00000376883.1:c.1311T>A	ENSP00000366080.1:p.Asp437Glu
ENST00000488757.5:c.1371T>A	ENSP00000418259.1:p.Asp457Glu
NM_001109809.2:c.1371T>A	NP_001103279.2:p.Asp457Glu
XM_006715087.2:c.1155T>A	XP_006715150.1:p.Asp385Glu
XM_011514570.1:c.1371T>A	XP_011512872.1:p.Asp457Glu
NM_001109809.3:c.1371T>A	NP_001103279.2:p.Asp457Glu
NM_001366333.1:c.1155T>A	NP_001353262.1:p.Asp385Glu
NM_001109809.4:c.1371T>A	NP_001103279.2:p.Asp457Glu
NM_001366333.2:c.1155T>A	NP_001353262.1:p.Asp385Glu
NM_001109809.5:c.1371T>A MANE Select	NP_001103279.2:p.Asp457Glu