Canonical Allele Identifier: CA347963758
Community Standard Title: NM_001386135.1(AFF3):c.698C>T (p.Ala233Val)
Gene: AFF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100006807G>A , CM000664.2:g.100006807G>A GRCh38
NC_000002.11:g.100623269G>A , CM000664.1:g.100623269G>A GRCh37
NC_000002.10:g.99989701G>A NCBI36
NG_052835.1:g.140777C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001386135.1:c.698C>T MANE Select NP_001373064.1:p.Ala233Val
ENST00000672756.2:c.698C>T MANE Select ENSP00000500419.1:p.Ala233Val
NM_001025108.1:c.773C>T NP_001020279.1:p.Ala258Val
NM_001025108.2:c.773C>T NP_001020279.1:p.Ala258Val
NM_002285.2:c.698C>T NP_002276.2:p.Ala233Val
NM_002285.3:c.698C>T NP_002276.2:p.Ala233Val
ENST00000317233.8:c.698C>T ENSP00000317421.4:p.Ala233Val
ENST00000409236.6:c.698C>T ENSP00000387207.1:p.Ala233Val
ENST00000409579.5:c.773C>T ENSP00000386834.1:p.Ala258Val
ENST00000430789.1:c.39C>T
ENST00000498090.1:n.1015C>T
ENST00000672204.1:c.698C>T ENSP00000500616.1:p.Ala233Val
ENST00000672269.1:c.773C>T ENSP00000500310.1:p.Ala258Val
XM_005263943.2:c.698C>T XP_005264000.2:p.Ala233Val
XM_005263943.4:c.698C>T XP_005264000.2:p.Ala233Val
XM_011511169.1:c.773C>T XP_011509471.1:p.Ala258Val
XM_011511169.3:c.1160C>T XP_011509471.2:p.Ala387Val
XM_011511170.1:c.929C>T XP_011509472.1:p.Ala310Val
XM_011511170.2:c.929C>T XP_011509472.1:p.Ala310Val
XM_011511171.1:c.773C>T XP_011509473.1:p.Ala258Val
XM_011511171.3:c.1160C>T XP_011509473.2:p.Ala387Val
XM_011511172.1:c.773C>T XP_011509474.1:p.Ala258Val
XM_011511173.1:c.773C>T XP_011509475.1:p.Ala258Val
XM_011511173.3:c.773C>T XP_011509475.1:p.Ala258Val
XM_011511174.1:c.773C>T XP_011509476.1:p.Ala258Val
XM_011511174.3:c.773C>T XP_011509476.1:p.Ala258Val
XM_011511175.1:c.698C>T XP_011509477.1:p.Ala233Val
XM_011511175.3:c.698C>T XP_011509477.1:p.Ala233Val
XM_011511176.1:c.698C>T XP_011509478.1:p.Ala233Val
XM_011511176.3:c.698C>T XP_011509478.1:p.Ala233Val
XM_011511177.1:c.698C>T XP_011509479.1:p.Ala233Val
XM_011511177.3:c.698C>T XP_011509479.1:p.Ala233Val
XM_024452883.1:c.1160C>T XP_024308651.1:p.Ala387Val