Canonical Allele Identifier: CA1618398851

Gene: ZFP57

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29672705_29672706delinsTG , CM000668.2:g.29672705_29672706delinsTG	GRCh38
NC_000006.11:g.29640482_29640483delinsTG , CM000668.1:g.29640482_29640483delinsTG	GRCh37
NC_000006.10:g.29748461_29748462delinsTG	NCBI36
NG_013045.1:g.9449_9450delinsCA
NG_031873.1:g.20725_20726delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376883.2:c.1405_1406delinsCA MANE Select	ENSP00000366080.2:p.Gln469=
ENST00000488757.6:c.1189_1190delinsCA	ENSP00000418259.2:p.Gln397=
ENST00000376881.4:c.1153_1154delinsCA	ENSP00000366078.4:p.Gln385=
ENST00000376883.1:c.1345_1346delinsCA	ENSP00000366080.1:p.Gln449=
ENST00000488757.5:c.1405_1406delinsCA	ENSP00000418259.1:p.Gln469=
NM_001109809.2:c.1405_1406delinsCA	NP_001103279.2:p.Gln469=
XM_006715087.2:c.1189_1190delinsCA	XP_006715150.1:p.Gln397=
XM_011514570.1:c.1405_1406delinsCA	XP_011512872.1:p.Gln469=
NM_001109809.3:c.1405_1406delinsCA	NP_001103279.2:p.Gln469=
NM_001366333.1:c.1189_1190delinsCA	NP_001353262.1:p.Gln397=
NM_001109809.4:c.1405_1406delinsCA	NP_001103279.2:p.Gln469=
NM_001366333.2:c.1189_1190delinsCA	NP_001353262.1:p.Gln397=
NM_001109809.5:c.1405_1406delinsCA MANE Select	NP_001103279.2:p.Gln469=