Canonical Allele Identifier: CA2067718836

Gene: OASL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121022942G= , CM000674.2:g.121022942G=	GRCh38
NC_000012.11:g.121460745G= , CM000674.1:g.121460745G=	GRCh37
NC_000012.10:g.119945128G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000257570.10:c.1047+1048C= MANE Select	ENSP00000257570.4:n.1047+1048C=
ENST00000339275.10:c.*37+1048C=	ENSP00000341125.5:n.*37+1048C=
ENST00000620239.5:c.658-1884C=	ENSP00000479512.1:n.658-1884C=
ENST00000679655.1:c.1047+1048C=	ENSP00000506490.1:n.1047+1048C=
ENST00000680485.1:c.*279+1048C=	ENSP00000506721.1:n.*279+1048C=
ENST00000680620.1:c.1047+1048C=	ENSP00000505685.1:n.1047+1048C=
ENST00000680750.1:n.1591+1048C=
ENST00000681005.1:n.653+1048C=
ENST00000681590.1:c.*521+1048C=	ENSP00000506074.1:n.*521+1048C=
ENST00000257570.9:c.1047+1048C=	ENSP00000257570.4:n.1047+1048C=
ENST00000339275.9:c.*37+1048C=	ENSP00000341125.5:n.*37+1048C=
ENST00000620239.4:c.658-1884C=	ENSP00000479512.1:n.658-1884C=
NM_001261825.1:c.658-1884C=	NP_001248754.1:n.658-1884C=
NM_003733.3:c.1047+1048C=	NP_003724.1:n.1047+1048C=
NM_198213.2:c.*37+1048C=	NP_937856.1:n.*37+1048C=
XM_017020140.1:c.1047+1048C=	XP_016875629.1:n.1047+1048C=
XM_017020141.1:c.*37+1048C=	XP_016875630.1:n.*37+1048C=
NM_001261825.2:c.658-1884C=	NP_001248754.1:n.658-1884C=
NM_001395418.1:c.*37+1048C=	NP_001382347.1:n.*37+1048C=
NM_001395419.1:c.1047+1048C=	NP_001382348.1:n.1047+1048C=
NM_003733.4:c.1047+1048C= MANE Select	NP_003724.1:n.1047+1048C=
NM_198213.3:c.*37+1048C=	NP_937856.1:n.*37+1048C=