Canonical Allele Identifier: CA281196766

Gene: ZNF423

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.49618868T>G , CM000678.2:g.49618868T>G	GRCh38
NC_000016.9:g.49652779T>G , CM000678.1:g.49652779T>G	GRCh37
NC_000016.8:g.48210280T>G	NCBI36
NG_032972.1:g.244052A>C
NG_032972.2:g.244052A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001379286.1:c.3601+7302A>C MANE Select	NP_001366215.1:n.3601+7302A>C
ENST00000563137.7:c.3601+7302A>C MANE Select	ENSP00000455588.3:n.3601+7302A>C
NM_001271620.1:c.3397+7302A>C	NP_001258549.1:n.3397+7302A>C
NM_001271620.2:c.3397+7302A>C	NP_001258549.1:n.3397+7302A>C
NM_001330533.1:c.3226+7302A>C	NP_001317462.1:n.3226+7302A>C
NM_001330533.2:c.3226+7302A>C	NP_001317462.1:n.3226+7302A>C
NM_015069.3:c.3577+7302A>C	NP_055884.2:n.3577+7302A>C
NM_015069.4:c.3577+7302A>C	NP_055884.2:n.3577+7302A>C
NM_015069.5:c.3577+7302A>C	NP_055884.2:n.3577+7302A>C
ENST00000262383.6:c.3577+7302A>C	ENSP00000262383.2:n.3577+7302A>C
ENST00000535559.5:c.3226+7302A>C	ENSP00000442321.1:n.3226+7302A>C
ENST00000561648.5:c.3577+7302A>C	ENSP00000455426.1:n.3577+7302A>C
ENST00000562520.1:c.3397+7302A>C	ENSP00000457664.1:n.3397+7302A>C
ENST00000562871.5:c.3397+7302A>C	ENSP00000457928.1:n.3397+7302A>C
ENST00000563137.6:c.3397+7302A>C	ENSP00000455588.2:n.3397+7302A>C
ENST00000567169.5:c.3226+7302A>C	ENSP00000455061.1:n.3226+7302A>C
XM_005255856.3:c.3397+7302A>C	XP_005255913.1:n.3397+7302A>C
XM_005255856.4:c.3397+7302A>C	XP_005255913.1:n.3397+7302A>C
XM_005255857.3:c.3226+7302A>C	XP_005255914.1:n.3226+7302A>C
XM_006721171.2:c.3622+7302A>C	XP_006721234.1:n.3622+7302A>C
XM_006721171.4:c.3622+7302A>C	XP_006721234.1:n.3622+7302A>C
XM_011522962.1:c.3670+7302A>C	XP_011521264.1:n.3670+7302A>C
XM_017023076.2:c.3601+7302A>C	XP_016878565.1:n.3601+7302A>C
XM_017023077.1:c.3397+7302A>C	XP_016878566.1:n.3397+7302A>C
XM_017023078.1:c.3397+7302A>C	XP_016878567.1:n.3397+7302A>C