Canonical Allele Identifier: CA2573152832

Gene: ZNF469

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88435898del , CM000678.2:g.88435898del	GRCh38
NC_000016.9:g.88502306del , CM000678.1:g.88502306del	GRCh37
NC_000016.8:g.87029807del	NCBI36
NG_012236.2:g.13428del

Transcript Alleles

HGVS	Amino-acid Change
NM_001367624.2:c.8428del MANE Select	NP_001354553.1:p.Ala2810ArgfsTer?
ENST00000565624.3:c.8428del MANE Select	ENSP00000456500.2:p.Ala2810ArgfsTer?
NM_001127464.2:c.8344del	NP_001120936.2:p.Ala2782ArgfsTer?
NM_001367624.1:c.8428del	NP_001354553.1:p.Ala2810ArgfsTer?
ENST00000437464.1:c.8344del	ENSP00000402343.1:p.Ala2782ArgfsTer?
ENST00000565624.1:c.8428del	ENSP00000456500.1:p.Ala2810ArgfsTer?
XM_011523386.1:c.8428del	XP_011521688.1:p.Ala2810ArgfsTer?
XM_011523387.1:c.8428del	XP_011521689.1:p.Ala2810ArgfsTer?
XM_011523388.1:c.8428del	XP_011521690.1:p.Ala2810ArgfsTer?
XM_017023784.1:c.8428del	XP_016879273.1:p.Ala2810ArgfsTer?
XM_017023785.1:c.8428del	XP_016879274.1:p.Ala2810ArgfsTer?