Canonical Allele Identifier: CA1156080392

Gene: SDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028314_17028317delinsAATG , CM000663.2:g.17028314_17028317delinsAATG	GRCh38
NC_000001.10:g.17354809_17354812delinsAATG , CM000663.1:g.17354809_17354812delinsAATG	GRCh37
NC_000001.9:g.17227396_17227399delinsAATG	NCBI36
NG_012340.1:g.30854_30857delinsCATT , LRG_316:g.30854_30857delinsCATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.252+283_252+286delinsCATT	ENSP00000481376.2:n.252+283_252+286delinsCATT
ENST00000491274.6:c.381+283_381+286delinsCATT	ENSP00000480482.2:n.381+283_381+286delinsCATT
ENST00000375499.8:c.423+283_423+286delinsCATT MANE Select	ENSP00000364649.3:n.423+283_423+286delinsCATT
ENST00000375499.7:c.423+283_423+286delinsCATT	ENSP00000364649.3:n.423+283_423+286delinsCATT
ENST00000463045.2:c.252+283_252+286delinsCATT	ENSP00000481376.1:n.252+283_252+286delinsCATT
ENST00000475506.1:n.340+283_340+286delinsCATT
ENST00000485515.5:n.357+337_357+340delinsCATT
ENST00000491274.5:c.381+283_381+286delinsCATT	ENSP00000480482.1:n.381+283_381+286delinsCATT
NM_003000.2:c.423+283_423+286delinsCATT , LRG_316t1:c.423+283_423+286delinsCATT	NP_002991.2:n.423+283_423+286delinsCATT
NM_003000.3:c.423+283_423+286delinsCATT MANE Select	NP_002991.2:n.423+283_423+286delinsCATT