Canonical Allele Identifier: CA658658102

Gene: SDHD

Linked Data

• dbSNP Id: rs1555186981

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112088896_112088898delinsGCC , CM000673.2:g.112088896_112088898delinsGCC	GRCh38
NC_000011.9:g.111959620_111959622delinsGCC , CM000673.1:g.111959620_111959622delinsGCC	GRCh37
NC_000011.8:g.111464830_111464832delinsGCC	NCBI36
NG_012337.2:g.7050_7052delinsGCC
NG_033145.1:g.2901_2903delinsGGC
NG_012337.3:g.7050_7052delinsGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.199_201delinsGCC	ENSP00000432946.2:p.Thr67Ala
ENST00000534010.2:c.199_201delinsGCC	ENSP00000433202.2:p.Thr67Ala
ENST00000375549.8:c.199_201delinsGCC MANE Select	ENSP00000364699.3:p.Thr67Ala
ENST00000528021.6:c.199_201delinsGCC	ENSP00000432465.1:p.Thr67Ala
ENST00000640554.1:c.*271_*273delinsGCC	ENSP00000491141.1:n.*271_*273delinsGCC
ENST00000375549.7:c.199_201delinsGCC	ENSP00000364699.3:p.Thr67Ala
ENST00000525291.5:c.82_84delinsGCC	ENSP00000436669.1:p.Thr28Ala
ENST00000525987.5:n.204_206delinsGCC
ENST00000526592.5:c.199_201delinsGCC	ENSP00000432005.1:p.Thr67Ala
ENST00000528021.5:c.199_201delinsGCC	ENSP00000432465.1:p.Thr67Ala
ENST00000528048.5:c.169+923_169+925delinsGCC	ENSP00000436217.1:n.169+923_169+925delinsGCC
ENST00000528182.5:c.199_201delinsGCC	ENSP00000435475.1:p.Thr67Ala
ENST00000530923.5:c.189_191delinsGCC
ENST00000531744.5:c.199_201delinsGCC	ENSP00000456957.1:p.Thr67Ala
ENST00000532699.1:c.199_201delinsGCC	ENSP00000456434.1:p.Thr67Ala
ENST00000534010.1:c.30_32delinsGCC
ENST00000614349.4:c.199_201delinsGCC	ENSP00000480666.1:p.Thr67Ala
NM_001276503.1:c.169+923_169+925delinsGCC	NP_001263432.1:n.169+923_169+925delinsGCC
NM_001276504.1:c.82_84delinsGCC	NP_001263433.1:p.Thr28Ala
NM_001276506.1:c.199_201delinsGCC	NP_001263435.1:p.Thr67Ala
NM_003002.3:c.199_201delinsGCC	NP_002993.1:p.Thr67Ala
NR_077060.1:n.283_285delinsGCC
NM_003002.4:c.199_201delinsGCC MANE Select	NP_002993.1:p.Thr67Ala
NM_001276503.2:c.169+923_169+925delinsGCC	NP_001263432.1:n.169+923_169+925delinsGCC
NM_001276504.2:c.82_84delinsGCC	NP_001263433.1:p.Thr28Ala
NM_001276506.2:c.199_201delinsGCC	NP_001263435.1:p.Thr67Ala
NR_077060.2:n.234_236delinsGCC