Canonical Allele Identifier: CA2000561018
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112087938_112087964delinsGAGTGCAGCACATACACTTGTCACCGA , CM000673.2:g.112087938_112087964delinsGAGTGCAGCACATACACTTGTCACCGA GRCh38
NC_000011.9:g.111958662_111958688delinsGAGTGCAGCACATACACTTGTCACCGA , CM000673.1:g.111958662_111958688delinsGAGTGCAGCACATACACTTGTCACCGA GRCh37
NC_000011.8:g.111463872_111463898delinsGAGTGCAGCACATACACTTGTCACCGA NCBI36
NG_012337.2:g.6092_6118delinsGAGTGCAGCACATACACTTGTCACCGA
NG_033145.1:g.3835_3861delinsTCGGTGACAAGTGTATGTGCTGCACTC
NG_012337.3:g.6092_6118delinsGAGTGCAGCACATACACTTGTCACCGA

Transcript Alleles

HGVS Amino-acid change
ENST00000530923.6:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000432946.2:p.Gly45=
ENST00000534010.2:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000433202.2:p.Gly45=
ENST00000375549.8:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA MANE Select ENSP00000364699.3:p.Gly45=
ENST00000528021.6:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000432465.1:p.Gly45=
ENST00000640554.1:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000491141.1:p.Gly45=
ENST00000375549.7:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000364699.3:p.Gly45=
ENST00000525291.5:c.53-929_53-903delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000436669.1:n.53-929_53-903delinsGA...
ENST00000525987.5:n.139_165delinsGAGTGCAGCACATACACTTGTCACCGA
ENST00000526592.5:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000432005.1:p.Gly45=
ENST00000528021.5:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000432465.1:p.Gly45=
ENST00000528048.5:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000436217.1:p.Gly45=
ENST00000528182.5:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000435475.1:p.Gly45=
ENST00000530923.5:c.124_150delinsGAGTGCAGCACATACACTTGTCACCGA
ENST00000531744.5:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000456957.1:p.Gly45=
ENST00000532699.1:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000456434.1:p.Gly45=
ENST00000614349.4:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA ENSP00000480666.1:p.Gly45=
NM_001276503.1:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA NP_001263432.1:p.Gly45=
NM_001276504.1:c.53-929_53-903delinsGAGTGCAGCACATACACTTGTCACCGA NP_001263433.1:n.53-929_53-903delinsGAGTG...
NM_001276506.1:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA NP_001263435.1:p.Gly45=
NM_003002.3:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA NP_002993.1:p.Gly45=
NR_077060.1:n.218_244delinsGAGTGCAGCACATACACTTGTCACCGA
NM_003002.4:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA MANE Select NP_002993.1:p.Gly45=
NM_001276503.2:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA NP_001263432.1:p.Gly45=
NM_001276504.2:c.53-929_53-903delinsGAGTGCAGCACATACACTTGTCACCGA NP_001263433.1:n.53-929_53-903delinsGAGTG...
NM_001276506.2:c.134_160delinsGAGTGCAGCACATACACTTGTCACCGA NP_001263435.1:p.Gly45=
NR_077060.2:n.169_195delinsGAGTGCAGCACATACACTTGTCACCGA