Canonical Allele Identifier: CA2615987113

Gene: SDHD

Linked Data

• gnomAD v4: 11-112095075-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095075G>A , CM000673.2:g.112095075G>A	GRCh38
NC_000011.9:g.111965799G>A , CM000673.1:g.111965799G>A	GRCh37
NC_000011.8:g.111471009G>A	NCBI36
NG_012337.2:g.13229G>A
NG_012337.3:g.13229G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*324G>A	ENSP00000432946.2:n.*324G>A
ENST00000534010.2:c.314+6064G>A	ENSP00000433202.2:n.314+6064G>A
ENST00000375549.8:c.*105G>A MANE Select	ENSP00000364699.3:n.*105G>A
ENST00000528021.6:c.314+6064G>A	ENSP00000432465.1:n.314+6064G>A
ENST00000375549.7:c.*105G>A	ENSP00000364699.3:n.*105G>A
ENST00000525291.5:c.*105G>A	ENSP00000436669.1:n.*105G>A
ENST00000525987.5:n.319+6064G>A
ENST00000526592.5:c.*283G>A	ENSP00000432005.1:n.*283G>A
ENST00000528021.5:c.314+6064G>A	ENSP00000432465.1:n.314+6064G>A
ENST00000528048.5:c.*182G>A	ENSP00000436217.1:n.*182G>A
ENST00000528182.5:c.*182G>A	ENSP00000435475.1:n.*182G>A
ENST00000530923.5:c.629G>A
ENST00000531744.5:c.314+6064G>A	ENSP00000456957.1:n.314+6064G>A
ENST00000532699.1:c.314+6064G>A	ENSP00000456434.1:n.314+6064G>A
ENST00000534010.1:c.145+6064G>A
NM_001276503.1:c.*182G>A	NP_001263432.1:n.*182G>A
NM_001276504.1:c.*105G>A	NP_001263433.1:n.*105G>A
NM_001276506.1:c.*283G>A	NP_001263435.1:n.*283G>A
NM_003002.3:c.*105G>A	NP_002993.1:n.*105G>A
NR_077060.1:n.723G>A
NM_003002.4:c.*105G>A MANE Select	NP_002993.1:n.*105G>A
NM_001276503.2:c.*182G>A	NP_001263432.1:n.*182G>A
NM_001276504.2:c.*105G>A	NP_001263433.1:n.*105G>A
NM_001276506.2:c.*283G>A	NP_001263435.1:n.*283G>A
NR_077060.2:n.674G>A