Canonical Allele Identifier: CA414510047

Gene: AFF2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.148662538C>T , CM000685.2:g.148662538C>T	GRCh38
NC_000023.10:g.147744059C>T , CM000685.1:g.147744059C>T	GRCh37
NC_000023.9:g.147551751C>T	NCBI36
NG_016313.1:g.166921C>T
NG_016313.2:g.166920C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370460.7:c.811C>T MANE Select	ENSP00000359489.2:p.Pro271Ser
ENST00000342251.7:c.799C>T	ENSP00000345459.4:p.Pro267Ser
ENST00000370457.9:c.811C>T	ENSP00000359486.6:p.Pro271Ser
ENST00000370458.5:c.799C>T	ENSP00000359487.1:p.Pro267Ser
ENST00000370460.6:c.811C>T	ENSP00000359489.2:p.Pro271Ser
NM_001169122.1:c.799C>T	NP_001162593.1:p.Pro267Ser
NM_001169123.1:c.799C>T	NP_001162594.1:p.Pro267Ser
NM_001169124.1:c.811C>T	NP_001162595.1:p.Pro271Ser
NM_001169125.1:c.799C>T	NP_001162596.1:p.Pro267Ser
NM_002025.3:c.811C>T	NP_002016.2:p.Pro271Ser
NM_001169122.2:c.799C>T	NP_001162593.1:p.Pro267Ser
NM_001169123.2:c.799C>T	NP_001162594.1:p.Pro267Ser
NM_001169124.2:c.811C>T	NP_001162595.1:p.Pro271Ser
NM_001169125.2:c.799C>T	NP_001162596.1:p.Pro267Ser
NM_002025.4:c.811C>T MANE Select	NP_002016.2:p.Pro271Ser