Canonical Allele Identifier: CA2997843

Gene: AFF1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87046247A>G , CM000666.2:g.87046247A>G	GRCh38
NC_000004.11:g.87967399A>G , CM000666.1:g.87967399A>G	GRCh37
NC_000004.10:g.88186423A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001166693.3:c.120A>G MANE Select	NP_001160165.1:p.Ala40=
ENST00000395146.9:c.120A>G MANE Select	ENSP00000378578.4:p.Ala40=
NM_001166693.1:c.120A>G	NP_001160165.1:p.Ala40=
NM_001166693.2:c.120A>G	NP_001160165.1:p.Ala40=
NM_001313959.1:c.99A>G	NP_001300888.1:p.Ala33=
NM_001313959.2:c.99A>G	NP_001300888.1:p.Ala33=
NM_001313960.1:c.-48-37873A>G	NP_001300889.1:n.-48-37873A>G
NM_001313960.2:c.-48-37873A>G	NP_001300889.1:n.-48-37873A>G
NM_005935.2:c.99A>G	NP_005926.1:p.Ala33=
NM_005935.3:c.99A>G	NP_005926.1:p.Ala33=
NM_005935.4:c.99A>G	NP_005926.1:p.Ala33=
ENST00000307808.10:c.99A>G	ENSP00000305689.6:p.Ala33=
ENST00000395146.8:c.120A>G	ENSP00000378578.4:p.Ala40=
ENST00000503477.5:c.120A>G	ENSP00000424483.1:p.Ala40=
ENST00000504956.5:n.314-448A>G
ENST00000507468.5:c.120A>G	ENSP00000427593.1:p.Ala40=
ENST00000511442.1:c.-79A>G	ENSP00000425755.1:n.-79A>G
ENST00000511722.5:c.-45-37876A>G	ENSP00000424766.1:n.-45-37876A>G
ENST00000544085.5:c.99A>G	ENSP00000440843.2:p.Ala33=
ENST00000544085.6:c.99A>G	ENSP00000440843.3:p.Ala33=
ENST00000674009.1:c.120A>G	ENSP00000501252.1:p.Ala40=
XM_005263007.2:c.120A>G	XP_005263064.1:p.Ala40=
XM_005263007.3:c.120A>G	XP_005263064.1:p.Ala40=
XM_005263009.2:c.120A>G	XP_005263066.1:p.Ala40=
XM_005263009.4:c.120A>G	XP_005263066.1:p.Ala40=
XM_005263011.2:c.114A>G	XP_005263068.1:p.Ala38=
XM_005263011.3:c.114A>G	XP_005263068.1:p.Ala38=
XM_005263013.2:c.120A>G	XP_005263070.1:p.Ala40=
XM_005263013.4:c.120A>G	XP_005263070.1:p.Ala40=
XM_011531973.1:c.120A>G	XP_011530275.1:p.Ala40=
XM_011531973.3:c.120A>G	XP_011530275.1:p.Ala40=
XM_017008215.2:c.-48-37873A>G	XP_016863704.1:n.-48-37873A>G