Canonical Allele Identifier: CA396110679

Gene: ZNF423

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.49491301G>A , CM000678.2:g.49491301G>A	GRCh38
NC_000016.9:g.49525212G>A , CM000678.1:g.49525212G>A	GRCh37
NC_000016.8:g.48082713G>A	NCBI36
NG_032972.1:g.371619C>T
NG_032972.2:g.371619C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001379286.1:c.3853C>T MANE Select	NP_001366215.1:p.His1285Tyr
ENST00000563137.7:c.3853C>T MANE Select	ENSP00000455588.3:p.His1285Tyr
NM_001271620.1:c.3649C>T	NP_001258549.1:p.His1217Tyr
NM_001271620.2:c.3649C>T	NP_001258549.1:p.His1217Tyr
NM_001330533.1:c.3478C>T	NP_001317462.1:p.His1160Tyr
NM_001330533.2:c.3478C>T	NP_001317462.1:p.His1160Tyr
NM_015069.3:c.3829C>T	NP_055884.2:p.His1277Tyr
NM_015069.4:c.3829C>T	NP_055884.2:p.His1277Tyr
NM_015069.5:c.3829C>T	NP_055884.2:p.His1277Tyr
ENST00000262383.6:c.3829C>T	ENSP00000262383.2:p.His1277Tyr
ENST00000535559.5:c.3478C>T	ENSP00000442321.1:p.His1160Tyr
ENST00000561648.5:c.3829C>T	ENSP00000455426.1:p.His1277Tyr
ENST00000562520.1:c.3649C>T	ENSP00000457664.1:p.His1217Tyr
ENST00000562871.5:c.3649C>T	ENSP00000457928.1:p.His1217Tyr
ENST00000563137.6:c.3649C>T	ENSP00000455588.2:p.His1217Tyr
ENST00000567169.5:c.3478C>T	ENSP00000455061.1:p.His1160Tyr
XM_005255856.3:c.3649C>T	XP_005255913.1:p.His1217Tyr
XM_005255856.4:c.3649C>T	XP_005255913.1:p.His1217Tyr
XM_005255857.3:c.3478C>T	XP_005255914.1:p.His1160Tyr
XM_006721171.2:c.3874C>T	XP_006721234.1:p.His1292Tyr
XM_006721171.4:c.3874C>T	XP_006721234.1:p.His1292Tyr
XM_011522962.1:c.3922C>T	XP_011521264.1:p.His1308Tyr
XM_017023076.2:c.3853C>T	XP_016878565.1:p.His1285Tyr
XM_017023077.1:c.3649C>T	XP_016878566.1:p.His1217Tyr
XM_017023078.1:c.3649C>T	XP_016878567.1:p.His1217Tyr