Canonical Allele Identifier: CA2241070028

Gene: ZNF469

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88427500_88427501delinsGC , CM000678.2:g.88427500_88427501delinsGC	GRCh38
NC_000016.9:g.88493908_88493909delinsGC , CM000678.1:g.88493908_88493909delinsGC	GRCh37
NC_000016.8:g.87021409_87021410delinsGC	NCBI36
NG_012236.2:g.5030_5031delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000565624.3:c.30_31delinsGC MANE Select	ENSP00000456500.2:p.Pro10=
ENST00000437464.1:c.30_31delinsGC	ENSP00000402343.1:p.Pro10=
ENST00000565624.1:c.30_31delinsGC	ENSP00000456500.1:p.Pro10=
NM_001127464.2:c.30_31delinsGC	NP_001120936.2:p.Pro10=
XM_011523386.1:c.30_31delinsGC	XP_011521688.1:p.Pro10=
XM_011523387.1:c.30_31delinsGC	XP_011521689.1:p.Pro10=
XM_011523388.1:c.30_31delinsGC	XP_011521690.1:p.Pro10=
XM_017023784.1:c.30_31delinsGC	XP_016879273.1:p.Pro10=
XM_017023785.1:c.30_31delinsGC	XP_016879274.1:p.Pro10=
XR_002957934.1:n.250+2463_250+2464delinsGC
NM_001367624.1:c.30_31delinsGC	NP_001354553.1:p.Pro10=
NM_001367624.2:c.30_31delinsGC MANE Select	NP_001354553.1:p.Pro10=