Canonical Allele Identifier: CA337003934

Gene: AFF2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.148967043C>T , CM000685.2:g.148967043C>T	GRCh38
NC_000023.10:g.148048573C>T , CM000685.1:g.148048573C>T	GRCh37
NC_000023.9:g.147856267C>T	NCBI36
NG_016313.1:g.471435C>T
NG_016313.2:g.471425C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370460.7:c.3167C>T MANE Select	ENSP00000359489.2:p.Thr1056Ile
ENST00000671877.1:n.2180C>T
ENST00000286437.7:c.2090C>T	ENSP00000286437.5:p.Thr697Ile
ENST00000342251.7:c.3062C>T	ENSP00000345459.4:p.Thr1021Ile
ENST00000370457.9:c.3062C>T	ENSP00000359486.6:p.Thr1021Ile
ENST00000370460.6:c.3167C>T	ENSP00000359489.2:p.Thr1056Ile
NM_001169122.1:c.3062C>T	NP_001162593.1:p.Thr1021Ile
NM_001169123.1:c.3137C>T	NP_001162594.1:p.Thr1046Ile
NM_001169124.1:c.3062C>T	NP_001162595.1:p.Thr1021Ile
NM_001169125.1:c.3050C>T	NP_001162596.1:p.Thr1017Ile
NM_001170628.1:c.2090C>T	NP_001164099.1:p.Thr697Ile
NM_002025.3:c.3167C>T	NP_002016.2:p.Thr1056Ile
NM_001169122.2:c.3062C>T	NP_001162593.1:p.Thr1021Ile
NM_001169123.2:c.3137C>T	NP_001162594.1:p.Thr1046Ile
NM_001169124.2:c.3062C>T	NP_001162595.1:p.Thr1021Ile
NM_001169125.2:c.3050C>T	NP_001162596.1:p.Thr1017Ile
NM_002025.4:c.3167C>T MANE Select	NP_002016.2:p.Thr1056Ile