Canonical Allele Identifier: CA10638631

Gene: ZNF469

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88439596A>G , CM000678.2:g.88439596A>G	GRCh38
NC_000016.9:g.88506004A>G , CM000678.1:g.88506004A>G	GRCh37
NC_000016.8:g.87033505A>G	NCBI36
NG_012236.2:g.17126A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001367624.2:c.*264A>G MANE Select	NP_001354553.1:n.*264A>G
ENST00000565624.3:c.*264A>G MANE Select	ENSP00000456500.2:n.*264A>G
NM_001127464.2:c.12042A>G	NP_001120936.2:n.12042A>G
NM_001367624.1:c.12126A>G	NP_001354553.1:n.12126A>G
ENST00000437464.1:c.12042A>G	ENSP00000402343.1:n.12042A>G
ENST00000565624.1:c.12126A>G	ENSP00000456500.1:n.12126A>G
XM_011523386.1:c.*264A>G	XP_011521688.1:n.*264A>G
XM_011523387.1:c.*264A>G	XP_011521689.1:n.*264A>G
XM_011523388.1:c.*264A>G	XP_011521690.1:n.*264A>G
XM_017023784.1:c.*264A>G	XP_016879273.1:n.*264A>G
XM_017023785.1:c.*264A>G	XP_016879274.1:n.*264A>G