Canonical Allele Identifier: CA725571455

Gene: ZNF469

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88439160dup , CM000678.2:g.88439160dup	GRCh38
NC_000016.9:g.88505568dup , CM000678.1:g.88505568dup	GRCh37
NC_000016.8:g.87033069dup	NCBI36
NG_012236.2:g.16690dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001367624.2:c.11690dup MANE Select	NP_001354553.1:p.Arg3899GlufsTer17
ENST00000565624.3:c.11690dup MANE Select	ENSP00000456500.2:p.Arg3899GlufsTer17
NM_001127464.2:c.11606dup	NP_001120936.2:p.Arg3871GlufsTer17
NM_001367624.1:c.11690dup	NP_001354553.1:p.Arg3899GlufsTer17
ENST00000437464.1:c.11606dup	ENSP00000402343.1:p.Arg3871GlufsTer17
ENST00000565624.1:c.11690dup	ENSP00000456500.1:p.Arg3899GlufsTer17
XM_011523386.1:c.11690dup	XP_011521688.1:p.Arg3899GlufsTer17
XM_011523387.1:c.11690dup	XP_011521689.1:p.Arg3899GlufsTer17
XM_011523388.1:c.11690dup	XP_011521690.1:p.Arg3899GlufsTer17
XM_017023784.1:c.11690dup	XP_016879273.1:p.Arg3899GlufsTer17
XM_017023785.1:c.11690dup	XP_016879274.1:p.Arg3899GlufsTer17