Canonical Allele Identifier: CA8046657

Gene: ZNF423

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.49637607A>G , CM000678.2:g.49637607A>G	GRCh38
NC_000016.9:g.49671518A>G , CM000678.1:g.49671518A>G	GRCh37
NC_000016.8:g.48229019A>G	NCBI36
NG_032972.1:g.225313T>C
NG_032972.2:g.225313T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563137.7:c.1569T>C MANE Select	ENSP00000455588.3:p.Asn523=
ENST00000262383.6:c.1545T>C	ENSP00000262383.2:p.Asn515=
ENST00000535559.5:c.1194T>C	ENSP00000442321.1:p.Asn398=
ENST00000561648.5:c.1545T>C	ENSP00000455426.1:p.Asn515=
ENST00000562520.1:c.1365T>C	ENSP00000457664.1:p.Asn455=
ENST00000562871.5:c.1365T>C	ENSP00000457928.1:p.Asn455=
ENST00000563137.6:c.1365T>C	ENSP00000455588.2:p.Asn455=
ENST00000567169.5:c.1194T>C	ENSP00000455061.1:p.Asn398=
NM_001271620.1:c.1365T>C	NP_001258549.1:p.Asn455=
NM_015069.3:c.1545T>C	NP_055884.2:p.Asn515=
XM_005255856.3:c.1365T>C	XP_005255913.1:p.Asn455=
XM_005255857.3:c.1194T>C	XP_005255914.1:p.Asn398=
XM_006721171.2:c.1590T>C	XP_006721234.1:p.Asn530=
XM_011522962.1:c.1638T>C	XP_011521264.1:p.Asn546=
NM_001271620.2:c.1365T>C	NP_001258549.1:p.Asn455=
NM_001330533.1:c.1194T>C	NP_001317462.1:p.Asn398=
NM_015069.4:c.1545T>C	NP_055884.2:p.Asn515=
XM_005255856.4:c.1365T>C	XP_005255913.1:p.Asn455=
XM_006721171.4:c.1590T>C	XP_006721234.1:p.Asn530=
XM_017023076.2:c.1569T>C	XP_016878565.1:p.Asn523=
XM_017023077.1:c.1365T>C	XP_016878566.1:p.Asn455=
XM_017023078.1:c.1365T>C	XP_016878567.1:p.Asn455=
NM_001330533.2:c.1194T>C	NP_001317462.1:p.Asn398=
NM_001379286.1:c.1569T>C MANE Select	NP_001366215.1:p.Asn523=
NM_015069.5:c.1545T>C	NP_055884.2:p.Asn515=