Canonical Allele Identifier: CA1399189112

Gene: ZNF148

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.125232850G= , CM000665.2:g.125232850G=	GRCh38
NC_000003.11:g.124951694G= , CM000665.1:g.124951694G=	GRCh37
NC_000003.10:g.126434384G=	NCBI36
NG_052987.1:g.147505C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000471196.2:c.1876C=	ENSP00000420038.2:p.Pro626=
ENST00000700044.1:c.1876C=	ENSP00000514760.1:p.Pro626=
ENST00000360647.9:c.1876C= MANE Select	ENSP00000353863.4:p.Pro626=
ENST00000360647.8:c.1876C=	ENSP00000353863.4:p.Pro626=
ENST00000468369.5:c.122-196C=	ENSP00000420102.1:n.122-196C=
ENST00000484491.5:c.1876C=	ENSP00000420335.1:p.Pro626=
ENST00000485866.5:c.1876C=	ENSP00000420448.1:p.Pro626=
ENST00000492394.5:c.1876C=	ENSP00000419322.1:p.Pro626=
ENST00000496732.1:n.174-196C=
ENST00000497929.1:n.1872C=
ENST00000544464.5:c.*509C=	ENSP00000437916.2:n.*509C=
NM_021964.2:c.1876C=	NP_068799.2:p.Pro626=
NM_001348424.1:c.1876C=	NP_001335353.1:p.Pro626=
NM_001348425.2:c.1876C=	NP_001335354.1:p.Pro626=
NM_001348426.2:c.1876C=	NP_001335355.1:p.Pro626=
NM_001348427.2:c.1876C=	NP_001335356.1:p.Pro626=
NM_001348428.2:c.1876C=	NP_001335357.1:p.Pro626=
NM_001348429.2:c.1876C=	NP_001335358.1:p.Pro626=
NM_001348430.2:c.1876C=	NP_001335359.1:p.Pro626=
NM_001348431.2:c.1876C=	NP_001335360.1:p.Pro626=
NM_001348432.2:c.1876C=	NP_001335361.1:p.Pro626=
NM_001348433.2:c.1876C=	NP_001335362.1:p.Pro626=
NM_001348434.2:c.1750C=	NP_001335363.1:p.Pro584=
NM_021964.3:c.1876C= MANE Select	NP_068799.2:p.Pro626=