Canonical Allele Identifier: CA9819062

Gene: ZNF341

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33740990G>A , CM000682.2:g.33740990G>A	GRCh38
NC_000020.10:g.32328796G>A , CM000682.1:g.32328796G>A	GRCh37
NC_000020.9:g.31792457G>A	NCBI36
NG_053072.1:g.14231G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001282933.2:c.120G>A MANE Select	NP_001269862.1:p.Ala40=
ENST00000375200.6:c.120G>A MANE Select	ENSP00000364346.1:p.Ala40=
NM_001282933.1:c.120G>A	NP_001269862.1:p.Ala40=
NM_001282935.1:c.47G>A	NP_001269864.1:p.Arg16His
NM_001282935.2:c.47G>A	NP_001269864.1:p.Arg16His
NM_032819.4:c.120G>A	NP_116208.3:p.Ala40=
NM_032819.5:c.120G>A	NP_116208.3:p.Ala40=
NR_104259.1:n.382G>A
NR_104259.2:n.146G>A
ENST00000342427.6:c.120G>A	ENSP00000344308.2:p.Ala40=
ENST00000375200.5:c.120G>A	ENSP00000364346.1:p.Ala40=
ENST00000483118.5:c.120G>A	ENSP00000432933.1:p.Ala40=
ENST00000497876.5:c.120G>A	ENSP00000434423.1:p.Ala40=
ENST00000698694.1:c.120G>A	ENSP00000513875.1:p.Ala40=
XR_001754424.2:n.485G>A
XR_002958536.1:n.485G>A