Canonical Allele Identifier: CA2241073099

Gene: ZNF469

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88437447C= , CM000678.2:g.88437447C=	GRCh38
NC_000016.9:g.88503855C= , CM000678.1:g.88503855C=	GRCh37
NC_000016.8:g.87031356C=	NCBI36
NG_012236.2:g.14977C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565624.3:c.9977C= MANE Select	ENSP00000456500.2:p.Thr3326=
ENST00000437464.1:c.9893C=	ENSP00000402343.1:p.Thr3298=
ENST00000565624.1:c.9977C=	ENSP00000456500.1:p.Thr3326=
NM_001127464.2:c.9893C=	NP_001120936.2:p.Thr3298=
XM_011523386.1:c.9977C=	XP_011521688.1:p.Thr3326=
XM_011523387.1:c.9977C=	XP_011521689.1:p.Thr3326=
XM_011523388.1:c.9977C=	XP_011521690.1:p.Thr3326=
XM_017023784.1:c.9977C=	XP_016879273.1:p.Thr3326=
XM_017023785.1:c.9977C=	XP_016879274.1:p.Thr3326=
NM_001367624.1:c.9977C=	NP_001354553.1:p.Thr3326=
NM_001367624.2:c.9977C= MANE Select	NP_001354553.1:p.Thr3326=