Canonical Allele Identifier: CA414515024

Gene: AFF2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.148978367G>A , CM000685.2:g.148978367G>A	GRCh38
NC_000023.10:g.148059897G>A , CM000685.1:g.148059897G>A	GRCh37
NC_000023.9:g.147867581G>A	NCBI36
NG_016313.1:g.482759G>A
NG_016313.2:g.482749G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370460.7:c.3482G>A MANE Select	ENSP00000359489.2:p.Arg1161Gln
ENST00000671877.1:n.2495G>A
ENST00000286437.7:c.2405G>A	ENSP00000286437.5:p.Arg802Gln
ENST00000342251.7:c.3377G>A	ENSP00000345459.4:p.Arg1126Gln
ENST00000370457.9:c.3377G>A	ENSP00000359486.6:p.Arg1126Gln
ENST00000370460.6:c.3482G>A	ENSP00000359489.2:p.Arg1161Gln
NM_001169122.1:c.3377G>A	NP_001162593.1:p.Arg1126Gln
NM_001169123.1:c.3452G>A	NP_001162594.1:p.Arg1151Gln
NM_001169124.1:c.3377G>A	NP_001162595.1:p.Arg1126Gln
NM_001169125.1:c.3365G>A	NP_001162596.1:p.Arg1122Gln
NM_001170628.1:c.2405G>A	NP_001164099.1:p.Arg802Gln
NM_002025.3:c.3482G>A	NP_002016.2:p.Arg1161Gln
NM_001169122.2:c.3377G>A	NP_001162593.1:p.Arg1126Gln
NM_001169123.2:c.3452G>A	NP_001162594.1:p.Arg1151Gln
NM_001169124.2:c.3377G>A	NP_001162595.1:p.Arg1126Gln
NM_001169125.2:c.3365G>A	NP_001162596.1:p.Arg1122Gln
NM_002025.4:c.3482G>A MANE Select	NP_002016.2:p.Arg1161Gln