Canonical Allele Identifier: CA397124920
Gene: ZNF469 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88437329A>G , CM000678.2:g.88437329A>G GRCh38
NC_000016.9:g.88503737A>G , CM000678.1:g.88503737A>G GRCh37
NC_000016.8:g.87031238A>G NCBI36
NG_012236.2:g.14859A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000565624.3:c.9859A>G MANE Select ENSP00000456500.2:p.Thr3287Ala
ENST00000437464.1:c.9775A>G ENSP00000402343.1:p.Thr3259Ala
ENST00000565624.1:c.9859A>G ENSP00000456500.1:p.Thr3287Ala
NM_001127464.2:c.9775A>G NP_001120936.2:p.Thr3259Ala
XM_011523386.1:c.9859A>G XP_011521688.1:p.Thr3287Ala
XM_011523387.1:c.9859A>G XP_011521689.1:p.Thr3287Ala
XM_011523388.1:c.9859A>G XP_011521690.1:p.Thr3287Ala
XM_017023784.1:c.9859A>G XP_016879273.1:p.Thr3287Ala
XM_017023785.1:c.9859A>G XP_016879274.1:p.Thr3287Ala
NM_001367624.1:c.9859A>G NP_001354553.1:p.Thr3287Ala
NM_001367624.2:c.9859A>G MANE Select NP_001354553.1:p.Thr3287Ala