Canonical Allele Identifier: CA2221403153

Gene: ZNF423

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.49716879T= , CM000678.2:g.49716879T=	GRCh38
NC_000016.9:g.49750790T= , CM000678.1:g.49750790T=	GRCh37
NC_000016.8:g.48308291T=	NCBI36
NG_032972.1:g.146041A=
NG_032972.2:g.146041A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001379286.1:c.301+13892A= MANE Select	NP_001366215.1:n.301+13892A=
ENST00000563137.7:c.301+13892A= MANE Select	ENSP00000455588.3:n.301+13892A=
NM_001271620.1:c.97+13892A=	NP_001258549.1:n.97+13892A=
NM_001271620.2:c.97+13892A=	NP_001258549.1:n.97+13892A=
NM_015069.3:c.277+13892A=	NP_055884.2:n.277+13892A=
NM_015069.4:c.277+13892A=	NP_055884.2:n.277+13892A=
NM_015069.5:c.277+13892A=	NP_055884.2:n.277+13892A=
ENST00000262383.6:c.277+13892A=	ENSP00000262383.2:n.277+13892A=
ENST00000561648.5:c.277+13892A=	ENSP00000455426.1:n.277+13892A=
ENST00000562520.1:c.97+13892A=	ENSP00000457664.1:n.97+13892A=
ENST00000562871.5:c.97+13892A=	ENSP00000457928.1:n.97+13892A=
ENST00000563137.6:c.97+13892A=	ENSP00000455588.2:n.97+13892A=
XM_005255856.3:c.97+13892A=	XP_005255913.1:n.97+13892A=
XM_005255856.4:c.97+13892A=	XP_005255913.1:n.97+13892A=
XM_006721171.2:c.322+13892A=	XP_006721234.1:n.322+13892A=
XM_006721171.4:c.322+13892A=	XP_006721234.1:n.322+13892A=
XM_011522962.1:c.370+13892A=	XP_011521264.1:n.370+13892A=
XM_017023076.2:c.301+13892A=	XP_016878565.1:n.301+13892A=
XM_017023077.1:c.97+13892A=	XP_016878566.1:n.97+13892A=
XM_017023078.1:c.97+13892A=	XP_016878567.1:n.97+13892A=