Canonical Allele Identifier: CA10537070

Gene: AFF2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.148955903A>G , CM000685.2:g.148955903A>G	GRCh38
NC_000023.10:g.148037433A>G , CM000685.1:g.148037433A>G	GRCh37
NC_000023.9:g.147845133A>G	NCBI36
NG_016313.1:g.460295A>G
NG_016313.2:g.460285A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002025.4:c.1858A>G MANE Select	NP_002016.2:p.Thr620Ala
ENST00000370460.7:c.1858A>G MANE Select	ENSP00000359489.2:p.Thr620Ala
NM_001169122.1:c.1759A>G	NP_001162593.1:p.Thr587Ala
NM_001169122.2:c.1759A>G	NP_001162593.1:p.Thr587Ala
NM_001169123.1:c.1828A>G	NP_001162594.1:p.Thr610Ala
NM_001169123.2:c.1828A>G	NP_001162594.1:p.Thr610Ala
NM_001169124.1:c.1753A>G	NP_001162595.1:p.Thr585Ala
NM_001169124.2:c.1753A>G	NP_001162595.1:p.Thr585Ala
NM_001169125.1:c.1741A>G	NP_001162596.1:p.Thr581Ala
NM_001169125.2:c.1741A>G	NP_001162596.1:p.Thr581Ala
NM_001170628.1:c.781A>G	NP_001164099.1:p.Thr261Ala
NM_002025.3:c.1858A>G	NP_002016.2:p.Thr620Ala
ENST00000286437.7:c.781A>G	ENSP00000286437.5:p.Thr261Ala
ENST00000342251.7:c.1759A>G	ENSP00000345459.4:p.Thr587Ala
ENST00000370457.9:c.1753A>G	ENSP00000359486.6:p.Thr585Ala
ENST00000370460.6:c.1858A>G	ENSP00000359489.2:p.Thr620Ala
ENST00000671877.1:n.871A>G