Canonical Allele Identifier: CA1977300955

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446003A= , CM000673.2:g.61446003A=	GRCh38
NC_000011.9:g.61213475A= , CM000673.1:g.61213475A=	GRCh37
NC_000011.8:g.60970051A=	NCBI36
NG_023393.1:g.20879A= , LRG_519:g.20879A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.433A= MANE Select	ENSP00000301761.3:p.Lys145=
ENST00000301761.6:c.433A=	ENSP00000301761.2:p.Lys145=
ENST00000359614.9:c.*141A=	ENSP00000352630.5:n.*141A=
ENST00000536670.5:n.396+7890A=
ENST00000537782.5:c.*79A=	ENSP00000469951.1:n.*79A=
ENST00000538594.5:c.370+7890A=	ENSP00000440939.1:n.370+7890A=
ENST00000541135.5:c.377+7883A=	ENSP00000443130.1:n.377+7883A=
ENST00000542074.1:c.*12A=	ENSP00000469670.1:n.*12A=
ENST00000542794.5:c.*435A=	ENSP00000439983.1:n.*435A=
ENST00000543044.2:c.397A=	ENSP00000440219.1:p.Lys133=
ENST00000543265.1:c.*56A=	ENSP00000443660.1:n.*56A=
ENST00000544025.5:n.465+7890A=
ENST00000544801.5:c.370+7890A=	ENSP00000442581.1:n.370+7890A=
ENST00000544880.1:n.374+7890A=
NM_017841.2:c.433A= , LRG_519t1:c.433A=	NP_060311.1:p.Lys145=
NM_017841.4:c.433A= MANE Select	NP_060311.1:p.Lys145=