Canonical Allele Identifier: CA495444771
Gene: ZNF423 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49636116G>A , CM000678.2:g.49636116G>A GRCh38
NC_000016.9:g.49670027G>A , CM000678.1:g.49670027G>A GRCh37
NC_000016.8:g.48227528G>A NCBI36
NG_032972.1:g.226804C>T
NG_032972.2:g.226804C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000563137.7:c.3060C>T MANE Select ENSP00000455588.3:p.Asp1020=
ENST00000262383.6:c.3036C>T ENSP00000262383.2:p.Asp1012=
ENST00000535559.5:c.2685C>T ENSP00000442321.1:p.Asp895=
ENST00000561648.5:c.3036C>T ENSP00000455426.1:p.Asp1012=
ENST00000562520.1:c.2856C>T ENSP00000457664.1:p.Asp952=
ENST00000562871.5:c.2856C>T ENSP00000457928.1:p.Asp952=
ENST00000563137.6:c.2856C>T ENSP00000455588.2:p.Asp952=
ENST00000567169.5:c.2685C>T ENSP00000455061.1:p.Asp895=
NM_001271620.1:c.2856C>T NP_001258549.1:p.Asp952=
NM_015069.3:c.3036C>T NP_055884.2:p.Asp1012=
XM_005255856.3:c.2856C>T XP_005255913.1:p.Asp952=
XM_005255857.3:c.2685C>T XP_005255914.1:p.Asp895=
XM_006721171.2:c.3081C>T XP_006721234.1:p.Asp1027=
XM_011522962.1:c.3129C>T XP_011521264.1:p.Asp1043=
NM_001271620.2:c.2856C>T NP_001258549.1:p.Asp952=
NM_001330533.1:c.2685C>T NP_001317462.1:p.Asp895=
NM_015069.4:c.3036C>T NP_055884.2:p.Asp1012=
XM_005255856.4:c.2856C>T XP_005255913.1:p.Asp952=
XM_006721171.4:c.3081C>T XP_006721234.1:p.Asp1027=
XM_017023076.2:c.3060C>T XP_016878565.1:p.Asp1020=
XM_017023077.1:c.2856C>T XP_016878566.1:p.Asp952=
XM_017023078.1:c.2856C>T XP_016878567.1:p.Asp952=
NM_001330533.2:c.2685C>T NP_001317462.1:p.Asp895=
NM_001379286.1:c.3060C>T MANE Select NP_001366215.1:p.Asp1020=
NM_015069.5:c.3036C>T NP_055884.2:p.Asp1012=