Canonical Allele Identifier: CA2221351952

Gene: ZNF423

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.49609655G>C , CM000678.2:g.49609655G>C	GRCh38
NC_000016.9:g.49643566G>C , CM000678.1:g.49643566G>C	GRCh37
NC_000016.8:g.48201067G>C	NCBI36
NG_032972.1:g.253265C>G
NG_032972.2:g.253265C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563137.7:c.3601+16515C>G MANE Select	ENSP00000455588.3:n.3601+16515C>G
ENST00000262383.6:c.3577+16515C>G	ENSP00000262383.2:n.3577+16515C>G
ENST00000535559.5:c.3226+16515C>G	ENSP00000442321.1:n.3226+16515C>G
ENST00000561648.5:c.3577+16515C>G	ENSP00000455426.1:n.3577+16515C>G
ENST00000562520.1:c.3397+16515C>G	ENSP00000457664.1:n.3397+16515C>G
ENST00000562871.5:c.3397+16515C>G	ENSP00000457928.1:n.3397+16515C>G
ENST00000563137.6:c.3397+16515C>G	ENSP00000455588.2:n.3397+16515C>G
ENST00000567169.5:c.3226+16515C>G	ENSP00000455061.1:n.3226+16515C>G
NM_001271620.1:c.3397+16515C>G	NP_001258549.1:n.3397+16515C>G
NM_015069.3:c.3577+16515C>G	NP_055884.2:n.3577+16515C>G
XM_005255856.3:c.3397+16515C>G	XP_005255913.1:n.3397+16515C>G
XM_005255857.3:c.3226+16515C>G	XP_005255914.1:n.3226+16515C>G
XM_006721171.2:c.3622+16515C>G	XP_006721234.1:n.3622+16515C>G
XM_011522962.1:c.3670+16515C>G	XP_011521264.1:n.3670+16515C>G
NM_001271620.2:c.3397+16515C>G	NP_001258549.1:n.3397+16515C>G
NM_001330533.1:c.3226+16515C>G	NP_001317462.1:n.3226+16515C>G
NM_015069.4:c.3577+16515C>G	NP_055884.2:n.3577+16515C>G
XM_005255856.4:c.3397+16515C>G	XP_005255913.1:n.3397+16515C>G
XM_006721171.4:c.3622+16515C>G	XP_006721234.1:n.3622+16515C>G
XM_017023076.2:c.3601+16515C>G	XP_016878565.1:n.3601+16515C>G
XM_017023077.1:c.3397+16515C>G	XP_016878566.1:n.3397+16515C>G
XM_017023078.1:c.3397+16515C>G	XP_016878567.1:n.3397+16515C>G
NM_001330533.2:c.3226+16515C>G	NP_001317462.1:n.3226+16515C>G
NM_001379286.1:c.3601+16515C>G MANE Select	NP_001366215.1:n.3601+16515C>G
NM_015069.5:c.3577+16515C>G	NP_055884.2:n.3577+16515C>G