Canonical Allele Identifier: CA2241072349

Gene: ZNF469

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88436761_88436784del , CM000678.2:g.88436761_88436784del	GRCh38
NC_000016.9:g.88503169_88503192del , CM000678.1:g.88503169_88503192del	GRCh37
NC_000016.8:g.87030670_87030693del	NCBI36
NG_012236.2:g.14291_14314del

Transcript Alleles

HGVS	Amino-acid Change
NM_001367624.2:c.9291_9314del MANE Select	NP_001354553.1:p.Ala3098_Gly3105del
ENST00000565624.3:c.9291_9314del MANE Select	ENSP00000456500.2:p.Ala3098_Gly3105del
NM_001127464.2:c.9207_9230del	NP_001120936.2:p.Ala3070_Gly3077del
NM_001367624.1:c.9291_9314del	NP_001354553.1:p.Ala3098_Gly3105del
ENST00000437464.1:c.9207_9230del	ENSP00000402343.1:p.Ala3070_Gly3077del
ENST00000565624.1:c.9291_9314del	ENSP00000456500.1:p.Ala3098_Gly3105del
XM_011523386.1:c.9291_9314del	XP_011521688.1:p.Ala3098_Gly3105del
XM_011523387.1:c.9291_9314del	XP_011521689.1:p.Ala3098_Gly3105del
XM_011523388.1:c.9291_9314del	XP_011521690.1:p.Ala3098_Gly3105del
XM_017023784.1:c.9291_9314del	XP_016879273.1:p.Ala3098_Gly3105del
XM_017023785.1:c.9291_9314del	XP_016879274.1:p.Ala3098_Gly3105del