Canonical Allele Identifier: CA10536858

Gene: AFF2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.148662623C>T , CM000685.2:g.148662623C>T	GRCh38
NC_000023.10:g.147744144C>T , CM000685.1:g.147744144C>T	GRCh37
NC_000023.9:g.147551836C>T	NCBI36
NG_016313.1:g.167006C>T
NG_016313.2:g.167005C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370460.7:c.896C>T MANE Select	ENSP00000359489.2:p.Pro299Leu
ENST00000342251.7:c.884C>T	ENSP00000345459.4:p.Pro295Leu
ENST00000370457.9:c.896C>T	ENSP00000359486.6:p.Pro299Leu
ENST00000370458.5:c.884C>T	ENSP00000359487.1:p.Pro295Leu
ENST00000370460.6:c.896C>T	ENSP00000359489.2:p.Pro299Leu
NM_001169122.1:c.884C>T	NP_001162593.1:p.Pro295Leu
NM_001169123.1:c.884C>T	NP_001162594.1:p.Pro295Leu
NM_001169124.1:c.896C>T	NP_001162595.1:p.Pro299Leu
NM_001169125.1:c.884C>T	NP_001162596.1:p.Pro295Leu
NM_002025.3:c.896C>T	NP_002016.2:p.Pro299Leu
NM_001169122.2:c.884C>T	NP_001162593.1:p.Pro295Leu
NM_001169123.2:c.884C>T	NP_001162594.1:p.Pro295Leu
NM_001169124.2:c.896C>T	NP_001162595.1:p.Pro299Leu
NM_001169125.2:c.884C>T	NP_001162596.1:p.Pro295Leu
NM_002025.4:c.896C>T MANE Select	NP_002016.2:p.Pro299Leu