Canonical Allele Identifier: CA2241069916

Gene: ZNF469

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88427301C= , CM000678.2:g.88427301C=	GRCh38
NC_000016.9:g.88493709C= , CM000678.1:g.88493709C=	GRCh37
NC_000016.8:g.87021210C=	NCBI36
NG_012236.2:g.4831C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000565624.3:c.-126-44C= MANE Select	ENSP00000456500.2:n.-126-44C=
XM_011523386.1:c.-126-44C=	XP_011521688.1:n.-126-44C=
XM_011523387.1:c.-126-44C=	XP_011521689.1:n.-126-44C=
XM_011523388.1:c.-126-44C=	XP_011521690.1:n.-126-44C=
XM_017023784.1:c.-170C=	XP_016879273.1:n.-170C=
XM_017023785.1:c.-126-44C=	XP_016879274.1:n.-126-44C=
XR_002957934.1:n.250+2663G=
NM_001367624.2:c.-126-44C= MANE Select	NP_001354553.1:n.-126-44C=