Canonical Allele Identifier: CA2221444280

Gene: ZNF423

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.49796293A= , CM000678.2:g.49796293A=	GRCh38
NC_000016.9:g.49830204A= , CM000678.1:g.49830204A=	GRCh37
NC_000016.8:g.48387705A=	NCBI36
NG_032972.1:g.66627T=
NG_032972.2:g.66627T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001379286.1:c.41-6747T= MANE Select	NP_001366215.1:n.41-6747T=
ENST00000563137.7:c.41-6747T= MANE Select	ENSP00000455588.3:n.41-6747T=
NM_001271620.1:c.-164-6747T=	NP_001258549.1:n.-164-6747T=
NM_001271620.2:c.-164-6747T=	NP_001258549.1:n.-164-6747T=
NM_015069.3:c.17-6747T=	NP_055884.2:n.17-6747T=
NM_015069.4:c.17-6747T=	NP_055884.2:n.17-6747T=
NM_015069.5:c.17-6747T=	NP_055884.2:n.17-6747T=
ENST00000262383.6:c.17-6747T=	ENSP00000262383.2:n.17-6747T=
ENST00000561648.5:c.17-6747T=	ENSP00000455426.1:n.17-6747T=
ENST00000562520.1:c.-164-6747T=	ENSP00000457664.1:n.-164-6747T=
ENST00000563137.6:c.-164-6747T=	ENSP00000455588.2:n.-164-6747T=
XM_006721171.2:c.62-6747T=	XP_006721234.1:n.62-6747T=
XM_006721171.4:c.62-6747T=	XP_006721234.1:n.62-6747T=
XM_011522962.1:c.110-6747T=	XP_011521264.1:n.110-6747T=
XM_017023076.2:c.41-6747T=	XP_016878565.1:n.41-6747T=