Canonical Allele Identifier: CA363043359

Gene: ZFP57

Linked Data

• MyVariant Identifiers: chr6:g.29640519C>A (hg19) ; chr6:g.29672742C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672742C>A , CM000668.2:g.29672742C>A	GRCh38
NC_000006.11:g.29640519C>A , CM000668.1:g.29640519C>A	GRCh37
NC_000006.10:g.29748498C>A	NCBI36
NG_013045.1:g.9413G>T
NG_031873.1:g.20762C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000376883.2:c.1369G>T MANE Select	ENSP00000366080.2:p.Asp457Tyr
ENST00000488757.6:c.1153G>T	ENSP00000418259.2:p.Asp385Tyr
ENST00000376881.4:c.1117G>T	ENSP00000366078.4:p.Asp373Tyr
ENST00000376883.1:c.1309G>T	ENSP00000366080.1:p.Asp437Tyr
ENST00000488757.5:c.1369G>T	ENSP00000418259.1:p.Asp457Tyr
NM_001109809.2:c.1369G>T	NP_001103279.2:p.Asp457Tyr
XM_006715087.2:c.1153G>T	XP_006715150.1:p.Asp385Tyr
XM_011514570.1:c.1369G>T	XP_011512872.1:p.Asp457Tyr
NM_001109809.3:c.1369G>T	NP_001103279.2:p.Asp457Tyr
NM_001366333.1:c.1153G>T	NP_001353262.1:p.Asp385Tyr
NM_001109809.4:c.1369G>T	NP_001103279.2:p.Asp457Tyr
NM_001366333.2:c.1153G>T	NP_001353262.1:p.Asp385Tyr
NM_001109809.5:c.1369G>T MANE Select	NP_001103279.2:p.Asp457Tyr