Canonical Allele Identifier: CA8046692

Gene: ZNF423

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.49637787G>A , CM000678.2:g.49637787G>A	GRCh38
NC_000016.9:g.49671698G>A , CM000678.1:g.49671698G>A	GRCh37
NC_000016.8:g.48229199G>A	NCBI36
NG_032972.1:g.225133C>T
NG_032972.2:g.225133C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001379286.1:c.1389C>T MANE Select	NP_001366215.1:p.Asn463=
ENST00000563137.7:c.1389C>T MANE Select	ENSP00000455588.3:p.Asn463=
NM_001271620.1:c.1185C>T	NP_001258549.1:p.Asn395=
NM_001271620.2:c.1185C>T	NP_001258549.1:p.Asn395=
NM_001330533.1:c.1014C>T	NP_001317462.1:p.Asn338=
NM_001330533.2:c.1014C>T	NP_001317462.1:p.Asn338=
NM_015069.3:c.1365C>T	NP_055884.2:p.Asn455=
NM_015069.4:c.1365C>T	NP_055884.2:p.Asn455=
NM_015069.5:c.1365C>T	NP_055884.2:p.Asn455=
ENST00000262383.6:c.1365C>T	ENSP00000262383.2:p.Asn455=
ENST00000535559.5:c.1014C>T	ENSP00000442321.1:p.Asn338=
ENST00000561648.5:c.1365C>T	ENSP00000455426.1:p.Asn455=
ENST00000562520.1:c.1185C>T	ENSP00000457664.1:p.Asn395=
ENST00000562871.5:c.1185C>T	ENSP00000457928.1:p.Asn395=
ENST00000563137.6:c.1185C>T	ENSP00000455588.2:p.Asn395=
ENST00000567169.5:c.1014C>T	ENSP00000455061.1:p.Asn338=
XM_005255856.3:c.1185C>T	XP_005255913.1:p.Asn395=
XM_005255856.4:c.1185C>T	XP_005255913.1:p.Asn395=
XM_005255857.3:c.1014C>T	XP_005255914.1:p.Asn338=
XM_006721171.2:c.1410C>T	XP_006721234.1:p.Asn470=
XM_006721171.4:c.1410C>T	XP_006721234.1:p.Asn470=
XM_011522962.1:c.1458C>T	XP_011521264.1:p.Asn486=
XM_017023076.2:c.1389C>T	XP_016878565.1:p.Asn463=
XM_017023077.1:c.1185C>T	XP_016878566.1:p.Asn395=
XM_017023078.1:c.1185C>T	XP_016878567.1:p.Asn395=