Canonical Allele Identifier: CA10132296

Gene: PRAME

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.22548334A>G , CM000684.2:g.22548334A>G	GRCh38
NC_000022.10:g.22890756A>G , CM000684.1:g.22890756A>G	GRCh37
NC_000022.9:g.21220756A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_206956.3:c.1263T>C MANE Select	NP_996839.1:p.Ser421=
ENST00000405655.8:c.1263T>C MANE Select	ENSP00000384343.3:p.Ser421=
NM_001291715.1:c.1263T>C	NP_001278644.1:p.Ser421=
NM_001291715.2:c.1263T>C	NP_001278644.1:p.Ser421=
NM_001291716.1:c.1263T>C	NP_001278645.1:p.Ser421=
NM_001291716.2:c.1263T>C	NP_001278645.1:p.Ser421=
NM_001291717.1:c.1215T>C	NP_001278646.1:p.Ser405=
NM_001291717.2:c.1215T>C	NP_001278646.1:p.Ser405=
NM_001291719.1:c.1215T>C	NP_001278648.1:p.Ser405=
NM_001291719.2:c.1215T>C	NP_001278648.1:p.Ser405=
NM_001318126.1:c.1215T>C	NP_001305055.1:p.Ser405=
NM_001318126.2:c.1215T>C	NP_001305055.1:p.Ser405=
NM_001318127.1:c.1215T>C	NP_001305056.1:p.Ser405=
NM_001318127.2:c.1215T>C	NP_001305056.1:p.Ser405=
NM_006115.4:c.1263T>C	NP_006106.1:p.Ser421=
NM_006115.5:c.1263T>C	NP_006106.1:p.Ser421=
NM_206953.2:c.1263T>C	NP_996836.1:p.Ser421=
NM_206953.3:c.1263T>C	NP_996836.1:p.Ser421=
NM_206954.2:c.1263T>C	NP_996837.1:p.Ser421=
NM_206954.3:c.1263T>C	NP_996837.1:p.Ser421=
NM_206955.2:c.1263T>C	NP_996838.1:p.Ser421=
NM_206955.3:c.1263T>C	NP_996838.1:p.Ser421=
NM_206956.2:c.1263T>C	NP_996839.1:p.Ser421=
ENST00000398741.5:c.1263T>C	ENSP00000381726.1:p.Ser421=
ENST00000398743.6:c.1263T>C	ENSP00000381728.2:p.Ser421=
ENST00000402697.5:c.1263T>C	ENSP00000385198.1:p.Ser421=
ENST00000405655.7:c.1263T>C	ENSP00000384343.3:p.Ser421=
ENST00000492657.5:n.2198T>C
ENST00000543184.5:c.1263T>C	ENSP00000445675.1:p.Ser421=
XM_011530034.1:c.1215T>C	XP_011528336.1:p.Ser405=
XM_011530034.3:c.1215T>C	XP_011528336.1:p.Ser405=
XM_011530035.1:c.1215T>C	XP_011528337.1:p.Ser405=