Canonical Allele Identifier: CA15305501
Gene: AFF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87037243G>A , CM000666.2:g.87037243G>A GRCh38
NC_000004.11:g.87958395G>A , CM000666.1:g.87958395G>A GRCh37
NC_000004.10:g.88177419G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395146.9:c.39-8923G>A MANE Select ENSP00000378578.4:n.39-8923G>A
ENST00000544085.6:c.18-8923G>A ENSP00000440843.3:n.18-8923G>A
ENST00000674009.1:c.39-8923G>A ENSP00000501252.1:n.39-8923G>A
ENST00000307808.10:c.18-8923G>A ENSP00000305689.6:n.18-8923G>A
ENST00000395146.8:c.39-8923G>A ENSP00000378578.4:n.39-8923G>A
ENST00000503477.5:c.39-8923G>A ENSP00000424483.1:n.39-8923G>A
ENST00000504956.5:n.314-9452G>A
ENST00000507468.5:c.39-8923G>A ENSP00000427593.1:n.39-8923G>A
ENST00000511442.1:c.-160-8923G>A ENSP00000425755.1:n.-160-8923G>A
ENST00000511722.5:c.-46+29819G>A ENSP00000424766.1:n.-46+29819G>A
ENST00000544085.5:c.18-8923G>A ENSP00000440843.2:n.18-8923G>A
NM_001166693.1:c.39-8923G>A NP_001160165.1:n.39-8923G>A
NM_001166693.2:c.39-8923G>A NP_001160165.1:n.39-8923G>A
NM_001313959.1:c.18-8923G>A NP_001300888.1:n.18-8923G>A
NM_001313960.1:c.-49+29819G>A NP_001300889.1:n.-49+29819G>A
NM_005935.2:c.18-8923G>A NP_005926.1:n.18-8923G>A
NM_005935.3:c.18-8923G>A NP_005926.1:n.18-8923G>A
XM_005263007.2:c.39-8923G>A XP_005263064.1:n.39-8923G>A
XM_005263009.2:c.39-8923G>A XP_005263066.1:n.39-8923G>A
XM_005263011.2:c.33-8923G>A XP_005263068.1:n.33-8923G>A
XM_005263013.2:c.39-8923G>A XP_005263070.1:n.39-8923G>A
XM_011531973.1:c.39-8923G>A XP_011530275.1:n.39-8923G>A
XM_005263007.3:c.39-8923G>A XP_005263064.1:n.39-8923G>A
XM_005263009.4:c.39-8923G>A XP_005263066.1:n.39-8923G>A
XM_005263011.3:c.33-8923G>A XP_005263068.1:n.33-8923G>A
XM_005263013.4:c.39-8923G>A XP_005263070.1:n.39-8923G>A
XM_011531973.3:c.39-8923G>A XP_011530275.1:n.39-8923G>A
XM_017008215.2:c.-48-46877G>A XP_016863704.1:n.-48-46877G>A
NM_001166693.3:c.39-8923G>A MANE Select NP_001160165.1:n.39-8923G>A
NM_001313959.2:c.18-8923G>A NP_001300888.1:n.18-8923G>A
NM_001313960.2:c.-49+29819G>A NP_001300889.1:n.-49+29819G>A
NM_005935.4:c.18-8923G>A NP_005926.1:n.18-8923G>A
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