Canonical Allele Identifier: CA1977300638

Gene: SDHAF2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61445684C= , CM000673.2:g.61445684C=	GRCh38
NC_000011.9:g.61213156C= , CM000673.1:g.61213156C=	GRCh37
NC_000011.8:g.60969732C=	NCBI36
NG_023393.1:g.20560C= , LRG_519:g.20560C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.371-257C= MANE Select	ENSP00000301761.3:n.371-257C=
ENST00000301761.6:c.371-257C=	ENSP00000301761.2:n.371-257C=
ENST00000359614.9:c.*79-257C=	ENSP00000352630.5:n.*79-257C=
ENST00000536670.5:n.396+7571C=
ENST00000537782.5:c.*17-257C=	ENSP00000469951.1:n.*17-257C=
ENST00000538594.5:c.370+7571C=	ENSP00000440939.1:n.370+7571C=
ENST00000541135.5:c.377+7564C=	ENSP00000443130.1:n.377+7564C=
ENST00000542074.1:c.37-257C=	ENSP00000469670.1:n.37-257C=
ENST00000542794.5:c.*373-257C=	ENSP00000439983.1:n.*373-257C=
ENST00000543044.2:c.335-257C=	ENSP00000440219.1:n.335-257C=
ENST00000543265.1:c.261-257C=	ENSP00000443660.1:n.261-257C=
ENST00000544025.5:n.465+7571C=
ENST00000544801.5:c.370+7571C=	ENSP00000442581.1:n.370+7571C=
ENST00000544880.1:n.374+7571C=
NM_017841.2:c.371-257C= , LRG_519t1:c.371-257C=	NP_060311.1:n.371-257C=
NM_017841.4:c.371-257C= MANE Select	NP_060311.1:n.371-257C=