Canonical Allele Identifier: CA414516018
Community Standard Title: NM_002025.4(AFF2):c.2637G>T (p.Leu879Phe)
Gene: AFF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.148958405G>T , CM000685.2:g.148958405G>T GRCh38
NC_000023.10:g.148039935G>T , CM000685.1:g.148039935G>T GRCh37
NC_000023.9:g.147847635G>T NCBI36
NG_016313.1:g.462797G>T
NG_016313.2:g.462787G>T

Transcript Alleles

HGVS Amino-acid Change
NM_002025.4:c.2637G>T MANE Select NP_002016.2:p.Leu879Phe
ENST00000370460.7:c.2637G>T MANE Select ENSP00000359489.2:p.Leu879Phe
NM_001169122.1:c.2538G>T NP_001162593.1:p.Leu846Phe
NM_001169122.2:c.2538G>T NP_001162593.1:p.Leu846Phe
NM_001169123.1:c.2607G>T NP_001162594.1:p.Leu869Phe
NM_001169123.2:c.2607G>T NP_001162594.1:p.Leu869Phe
NM_001169124.1:c.2532G>T NP_001162595.1:p.Leu844Phe
NM_001169124.2:c.2532G>T NP_001162595.1:p.Leu844Phe
NM_001169125.1:c.2520G>T NP_001162596.1:p.Leu840Phe
NM_001169125.2:c.2520G>T NP_001162596.1:p.Leu840Phe
NM_001170628.1:c.1560G>T NP_001164099.1:p.Leu520Phe
NM_002025.3:c.2637G>T NP_002016.2:p.Leu879Phe
ENST00000286437.7:c.1560G>T ENSP00000286437.5:p.Leu520Phe
ENST00000342251.7:c.2538G>T ENSP00000345459.4:p.Leu846Phe
ENST00000370457.9:c.2532G>T ENSP00000359486.6:p.Leu844Phe
ENST00000370460.6:c.2637G>T ENSP00000359489.2:p.Leu879Phe
ENST00000671877.1:n.1650G>T