Canonical Allele Identifier: CA12203836
Gene: FOXO3 HGNC NCBI
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.108652895C>T , CM000668.2:g.108652895C>T GRCh38
NC_000006.11:g.108974098C>T , CM000668.1:g.108974098C>T GRCh37
NC_000006.10:g.109080791C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000406360.2:c.622-10560C>T MANE Select ENSP00000385824.1:n.622-10560C>T
ENST00000343882.10:c.622-10560C>T ENSP00000339527.6:n.622-10560C>T
ENST00000406360.1:c.622-10560C>T ENSP00000385824.1:n.622-10560C>T
NM_001455.3:c.622-10560C>T NP_001446.1:n.622-10560C>T
NM_201559.2:c.622-10560C>T NP_963853.1:n.622-10560C>T
XM_005266867.3:c.55-10560C>T XP_005266924.1:n.55-10560C>T
XM_011535626.1:c.121-10560C>T XP_011533928.1:n.121-10560C>T
XM_011535627.1:c.70-10560C>T XP_011533929.1:n.70-10560C>T
XM_011535628.1:c.-39-10560C>T XP_011533930.1:n.-39-10560C>T
XM_005266867.4:c.55-10560C>T XP_005266924.1:n.55-10560C>T
XM_011535626.2:c.121-10560C>T XP_011533928.1:n.121-10560C>T
XM_011535628.3:c.-39-10560C>T XP_011533930.1:n.-39-10560C>T
XM_017010585.1:c.55-10560C>T XP_016866074.1:n.55-10560C>T
XM_017010586.1:c.-39-10560C>T XP_016866075.1:n.-39-10560C>T
NM_001455.4:c.622-10560C>T MANE Select NP_001446.1:n.622-10560C>T
NM_201559.3:c.622-10560C>T NP_963853.1:n.622-10560C>T