Canonical Allele Identifier: CA2998172
Community Standard Title: NM_001166693.3(AFF1):c.1191+8C>T
Gene: AFF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87090078C>T , CM000666.2:g.87090078C>T GRCh38
NC_000004.11:g.88011230C>T , CM000666.1:g.88011230C>T GRCh37
NC_000004.10:g.88230254C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001166693.3:c.1191+8C>T MANE Select NP_001160165.1:n.1191+8C>T
ENST00000395146.9:c.1191+8C>T MANE Select ENSP00000378578.4:n.1191+8C>T
NM_001166693.1:c.1191+8C>T NP_001160165.1:n.1191+8C>T
NM_001166693.2:c.1191+8C>T NP_001160165.1:n.1191+8C>T
NM_001313959.1:c.1170+8C>T NP_001300888.1:n.1170+8C>T
NM_001313959.2:c.1170+8C>T NP_001300888.1:n.1170+8C>T
NM_001313960.1:c.84+8C>T NP_001300889.1:n.84+8C>T
NM_001313960.2:c.84+8C>T NP_001300889.1:n.84+8C>T
NM_005935.2:c.1170+8C>T NP_005926.1:n.1170+8C>T
NM_005935.3:c.1170+8C>T NP_005926.1:n.1170+8C>T
NM_005935.4:c.1170+8C>T NP_005926.1:n.1170+8C>T
ENST00000307808.10:c.1170+8C>T ENSP00000305689.6:n.1170+8C>T
ENST00000395146.8:c.1191+8C>T ENSP00000378578.4:n.1191+8C>T
ENST00000503477.5:c.1105-1715C>T ENSP00000424483.1:n.1105-1715C>T
ENST00000507468.5:c.1188+8C>T ENSP00000427593.1:n.1188+8C>T
ENST00000511722.5:c.84+8C>T ENSP00000424766.1:n.84+8C>T
ENST00000514970.2:c.243+8C>T ENSP00000424881.1:n.243+8C>T
ENST00000544085.5:c.1170+8C>T ENSP00000440843.2:n.1170+8C>T
ENST00000544085.6:c.1170+8C>T ENSP00000440843.3:n.1170+8C>T
ENST00000674009.1:c.1191+8C>T ENSP00000501252.1:n.1191+8C>T
XM_005263007.2:c.1191+8C>T XP_005263064.1:n.1191+8C>T
XM_005263007.3:c.1191+8C>T XP_005263064.1:n.1191+8C>T
XM_005263009.2:c.1188+8C>T XP_005263066.1:n.1188+8C>T
XM_005263009.4:c.1188+8C>T XP_005263066.1:n.1188+8C>T
XM_005263011.2:c.1185+8C>T XP_005263068.1:n.1185+8C>T
XM_005263011.3:c.1185+8C>T XP_005263068.1:n.1185+8C>T
XM_005263013.2:c.1191+8C>T XP_005263070.1:n.1191+8C>T
XM_005263013.4:c.1191+8C>T XP_005263070.1:n.1191+8C>T
XM_011531973.1:c.1191+8C>T XP_011530275.1:n.1191+8C>T
XM_011531973.3:c.1191+8C>T XP_011530275.1:n.1191+8C>T
XM_017008215.2:c.84+8C>T XP_016863704.1:n.84+8C>T
XM_017008216.1:c.84+8C>T XP_016863705.1:n.84+8C>T