Canonical Allele Identifier: CA2241070033

Gene: ZNF469

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88427507_88427508delinsAC , CM000678.2:g.88427507_88427508delinsAC	GRCh38
NC_000016.9:g.88493915_88493916delinsAC , CM000678.1:g.88493915_88493916delinsAC	GRCh37
NC_000016.8:g.87021416_87021417delinsAC	NCBI36
NG_012236.2:g.5037_5038delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000565624.3:c.37_38delinsAC MANE Select	ENSP00000456500.2:p.Thr13=
ENST00000437464.1:c.37_38delinsAC	ENSP00000402343.1:p.Thr13=
ENST00000565624.1:c.37_38delinsAC	ENSP00000456500.1:p.Thr13=
NM_001127464.2:c.37_38delinsAC	NP_001120936.2:p.Thr13=
XM_011523386.1:c.37_38delinsAC	XP_011521688.1:p.Thr13=
XM_011523387.1:c.37_38delinsAC	XP_011521689.1:p.Thr13=
XM_011523388.1:c.37_38delinsAC	XP_011521690.1:p.Thr13=
XM_017023784.1:c.37_38delinsAC	XP_016879273.1:p.Thr13=
XM_017023785.1:c.37_38delinsAC	XP_016879274.1:p.Thr13=
XR_002957934.1:n.250+2456_250+2457delinsGT
NM_001367624.1:c.37_38delinsAC	NP_001354553.1:p.Thr13=
NM_001367624.2:c.37_38delinsAC MANE Select	NP_001354553.1:p.Thr13=