Canonical Allele Identifier: CA281211179

Gene: ZNF423

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.49636255T>C , CM000678.2:g.49636255T>C	GRCh38
NC_000016.9:g.49670166T>C , CM000678.1:g.49670166T>C	GRCh37
NC_000016.8:g.48227667T>C	NCBI36
NG_032972.1:g.226665A>G
NG_032972.2:g.226665A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563137.7:c.2921A>G MANE Select	ENSP00000455588.3:p.Glu974Gly
ENST00000262383.6:c.2897A>G	ENSP00000262383.2:p.Glu966Gly
ENST00000535559.5:c.2546A>G	ENSP00000442321.1:p.Glu849Gly
ENST00000561648.5:c.2897A>G	ENSP00000455426.1:p.Glu966Gly
ENST00000562520.1:c.2717A>G	ENSP00000457664.1:p.Glu906Gly
ENST00000562871.5:c.2717A>G	ENSP00000457928.1:p.Glu906Gly
ENST00000563137.6:c.2717A>G	ENSP00000455588.2:p.Glu906Gly
ENST00000567169.5:c.2546A>G	ENSP00000455061.1:p.Glu849Gly
NM_001271620.1:c.2717A>G	NP_001258549.1:p.Glu906Gly
NM_015069.3:c.2897A>G	NP_055884.2:p.Glu966Gly
XM_005255856.3:c.2717A>G	XP_005255913.1:p.Glu906Gly
XM_005255857.3:c.2546A>G	XP_005255914.1:p.Glu849Gly
XM_006721171.2:c.2942A>G	XP_006721234.1:p.Glu981Gly
XM_011522962.1:c.2990A>G	XP_011521264.1:p.Glu997Gly
NM_001271620.2:c.2717A>G	NP_001258549.1:p.Glu906Gly
NM_001330533.1:c.2546A>G	NP_001317462.1:p.Glu849Gly
NM_015069.4:c.2897A>G	NP_055884.2:p.Glu966Gly
XM_005255856.4:c.2717A>G	XP_005255913.1:p.Glu906Gly
XM_006721171.4:c.2942A>G	XP_006721234.1:p.Glu981Gly
XM_017023076.2:c.2921A>G	XP_016878565.1:p.Glu974Gly
XM_017023077.1:c.2717A>G	XP_016878566.1:p.Glu906Gly
XM_017023078.1:c.2717A>G	XP_016878567.1:p.Glu906Gly
NM_001330533.2:c.2546A>G	NP_001317462.1:p.Glu849Gly
NM_001379286.1:c.2921A>G MANE Select	NP_001366215.1:p.Glu974Gly
NM_015069.5:c.2897A>G	NP_055884.2:p.Glu966Gly