Canonical Allele Identifier: CA2634824086

Gene: ZNF469

Linked Data

• gnomAD v4: 16-88427495-GCGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88427500_88427502del , CM000678.2:g.88427500_88427502del	GRCh38
NC_000016.9:g.88493908_88493910del , CM000678.1:g.88493908_88493910del	GRCh37
NC_000016.8:g.87021409_87021411del	NCBI36
NG_012236.2:g.5030_5032del

Transcript Alleles

HGVS	Amino-acid change
ENST00000565624.3:c.30_32del MANE Select	ENSP00000456500.2:p.Pro11del
ENST00000437464.1:c.30_32del	ENSP00000402343.1:p.Pro11del
ENST00000565624.1:c.30_32del	ENSP00000456500.1:p.Pro11del
NM_001127464.2:c.30_32del	NP_001120936.2:p.Pro11del
XM_011523386.1:c.30_32del	XP_011521688.1:p.Pro11del
XM_011523387.1:c.30_32del	XP_011521689.1:p.Pro11del
XM_011523388.1:c.30_32del	XP_011521690.1:p.Pro11del
XM_017023784.1:c.30_32del	XP_016879273.1:p.Pro11del
XM_017023785.1:c.30_32del	XP_016879274.1:p.Pro11del
XR_002957934.1:n.250+2466_250+2468del
NM_001367624.1:c.30_32del	NP_001354553.1:p.Pro11del
NM_001367624.2:c.30_32del MANE Select	NP_001354553.1:p.Pro11del