Canonical Allele Identifier: CA2615987126

Gene: SDHD

Linked Data

• gnomAD v4: 11-112095080-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095080C>A , CM000673.2:g.112095080C>A	GRCh38
NC_000011.9:g.111965804C>A , CM000673.1:g.111965804C>A	GRCh37
NC_000011.8:g.111471014C>A	NCBI36
NG_012337.2:g.13234C>A
NG_012337.3:g.13234C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*329C>A	ENSP00000432946.2:n.*329C>A
ENST00000534010.2:c.314+6069C>A	ENSP00000433202.2:n.314+6069C>A
ENST00000375549.8:c.*110C>A MANE Select	ENSP00000364699.3:n.*110C>A
ENST00000528021.6:c.314+6069C>A	ENSP00000432465.1:n.314+6069C>A
ENST00000375549.7:c.*110C>A	ENSP00000364699.3:n.*110C>A
ENST00000525291.5:c.*110C>A	ENSP00000436669.1:n.*110C>A
ENST00000525987.5:n.319+6069C>A
ENST00000526592.5:c.*288C>A	ENSP00000432005.1:n.*288C>A
ENST00000528021.5:c.314+6069C>A	ENSP00000432465.1:n.314+6069C>A
ENST00000528048.5:c.*187C>A	ENSP00000436217.1:n.*187C>A
ENST00000528182.5:c.*187C>A	ENSP00000435475.1:n.*187C>A
ENST00000530923.5:c.634C>A
ENST00000531744.5:c.314+6069C>A	ENSP00000456957.1:n.314+6069C>A
ENST00000532699.1:c.314+6069C>A	ENSP00000456434.1:n.314+6069C>A
ENST00000534010.1:c.145+6069C>A
NM_001276503.1:c.*187C>A	NP_001263432.1:n.*187C>A
NM_001276504.1:c.*110C>A	NP_001263433.1:n.*110C>A
NM_001276506.1:c.*288C>A	NP_001263435.1:n.*288C>A
NM_003002.3:c.*110C>A	NP_002993.1:n.*110C>A
NR_077060.1:n.728C>A
NM_003002.4:c.*110C>A MANE Select	NP_002993.1:n.*110C>A
NM_001276503.2:c.*187C>A	NP_001263432.1:n.*187C>A
NM_001276504.2:c.*110C>A	NP_001263433.1:n.*110C>A
NM_001276506.2:c.*288C>A	NP_001263435.1:n.*288C>A
NR_077060.2:n.679C>A