Canonical Allele Identifier: CA2241070021
Gene: ZNF469 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88427489C= , CM000678.2:g.88427489C= GRCh38
NC_000016.9:g.88493897C= , CM000678.1:g.88493897C= GRCh37
NC_000016.8:g.87021398C= NCBI36
NG_012236.2:g.5019C=

Transcript Alleles

HGVS Amino-acid change
ENST00000565624.3:c.19C= MANE Select ENSP00000456500.2:p.Arg7=
ENST00000437464.1:c.19C= ENSP00000402343.1:p.Arg7=
ENST00000565624.1:c.19C= ENSP00000456500.1:p.Arg7=
NM_001127464.2:c.19C= NP_001120936.2:p.Arg7=
XM_011523386.1:c.19C= XP_011521688.1:p.Arg7=
XM_011523387.1:c.19C= XP_011521689.1:p.Arg7=
XM_011523388.1:c.19C= XP_011521690.1:p.Arg7=
XM_017023784.1:c.19C= XP_016879273.1:p.Arg7=
XM_017023785.1:c.19C= XP_016879274.1:p.Arg7=
XR_002957934.1:n.250+2475G=
NM_001367624.1:c.19C= NP_001354553.1:p.Arg7=
NM_001367624.2:c.19C= MANE Select NP_001354553.1:p.Arg7=