Canonical Allele Identifier: CA1399188640

Gene: ZNF148

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.125232674C= , CM000665.2:g.125232674C=	GRCh38
NC_000003.11:g.124951518C= , CM000665.1:g.124951518C=	GRCh37
NC_000003.10:g.126434208C=	NCBI36
NG_052987.1:g.147681G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471196.2:c.2052G=	ENSP00000420038.2:p.Gln684=
ENST00000700044.1:c.2052G=	ENSP00000514760.1:p.Gln684=
ENST00000360647.9:c.2052G= MANE Select	ENSP00000353863.4:p.Gln684=
ENST00000360647.8:c.2052G=	ENSP00000353863.4:p.Gln684=
ENST00000468369.5:c.122-20G=	ENSP00000420102.1:n.122-20G=
ENST00000484491.5:c.2052G=	ENSP00000420335.1:p.Gln684=
ENST00000485866.5:c.2052G=	ENSP00000420448.1:p.Gln684=
ENST00000492394.5:c.2052G=	ENSP00000419322.1:p.Gln684=
ENST00000496732.1:n.174-20G=
ENST00000497929.1:n.2048G=
NM_021964.2:c.2052G=	NP_068799.2:p.Gln684=
NM_001348424.1:c.2052G=	NP_001335353.1:p.Gln684=
NM_001348425.2:c.2052G=	NP_001335354.1:p.Gln684=
NM_001348426.2:c.2052G=	NP_001335355.1:p.Gln684=
NM_001348427.2:c.2052G=	NP_001335356.1:p.Gln684=
NM_001348428.2:c.2052G=	NP_001335357.1:p.Gln684=
NM_001348429.2:c.2052G=	NP_001335358.1:p.Gln684=
NM_001348430.2:c.2052G=	NP_001335359.1:p.Gln684=
NM_001348431.2:c.2052G=	NP_001335360.1:p.Gln684=
NM_001348432.2:c.2052G=	NP_001335361.1:p.Gln684=
NM_001348433.2:c.2052G=	NP_001335362.1:p.Gln684=
NM_001348434.2:c.1926G=	NP_001335363.1:p.Gln642=
NM_021964.3:c.2052G= MANE Select	NP_068799.2:p.Gln684=