Canonical Allele Identifier: CA1618398864

Gene: ZFP57

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672745T= , CM000668.2:g.29672745T=	GRCh38
NC_000006.11:g.29640522T= , CM000668.1:g.29640522T=	GRCh37
NC_000006.10:g.29748501T=	NCBI36
NG_013045.1:g.9410A=
NG_031873.1:g.20765T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000376883.2:c.1366A= MANE Select	ENSP00000366080.2:p.Met456=
ENST00000488757.6:c.1150A=	ENSP00000418259.2:p.Met384=
ENST00000376881.4:c.1114A=	ENSP00000366078.4:p.Met372=
ENST00000376883.1:c.1306A=	ENSP00000366080.1:p.Met436=
ENST00000488757.5:c.1366A=	ENSP00000418259.1:p.Met456=
NM_001109809.2:c.1366A=	NP_001103279.2:p.Met456=
XM_006715087.2:c.1150A=	XP_006715150.1:p.Met384=
XM_011514570.1:c.1366A=	XP_011512872.1:p.Met456=
NM_001109809.3:c.1366A=	NP_001103279.2:p.Met456=
NM_001366333.1:c.1150A=	NP_001353262.1:p.Met384=
NM_001109809.4:c.1366A=	NP_001103279.2:p.Met456=
NM_001366333.2:c.1150A=	NP_001353262.1:p.Met384=
NM_001109809.5:c.1366A= MANE Select	NP_001103279.2:p.Met456=