Canonical Allele Identifier: CA1156080268

Gene: SDHB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027995_17027997delinsCTT , CM000663.2:g.17027995_17027997delinsCTT	GRCh38
NC_000001.10:g.17354490_17354492delinsCTT , CM000663.1:g.17354490_17354492delinsCTT	GRCh37
NC_000001.9:g.17227077_17227079delinsCTT	NCBI36
NG_012340.1:g.31174_31176delinsAAG , LRG_316:g.31174_31176delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.253-132_253-130delinsAAG	ENSP00000481376.2:n.253-132_253-130delinsAAG
ENST00000491274.6:c.382-132_382-130delinsAAG	ENSP00000480482.2:n.382-132_382-130delinsAAG
ENST00000375499.8:c.424-132_424-130delinsAAG MANE Select	ENSP00000364649.3:n.424-132_424-130delinsAAG
ENST00000375499.7:c.424-132_424-130delinsAAG	ENSP00000364649.3:n.424-132_424-130delinsAAG
ENST00000463045.2:c.253-132_253-130delinsAAG	ENSP00000481376.1:n.253-132_253-130delinsAAG
ENST00000475506.1:n.341-132_341-130delinsAAG
ENST00000485515.5:n.358-132_358-130delinsAAG
ENST00000491274.5:c.382-132_382-130delinsAAG	ENSP00000480482.1:n.382-132_382-130delinsAAG
NM_003000.2:c.424-132_424-130delinsAAG , LRG_316t1:c.424-132_424-130delinsAAG	NP_002991.2:n.424-132_424-130delinsAAG
NM_003000.3:c.424-132_424-130delinsAAG MANE Select	NP_002991.2:n.424-132_424-130delinsAAG