Canonical Allele Identifier: CA2615987383

Gene: SDHD

Linked Data

• gnomAD v4: 11-112095288-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095288C>A , CM000673.2:g.112095288C>A	GRCh38
NC_000011.9:g.111966012C>A , CM000673.1:g.111966012C>A	GRCh37
NC_000011.8:g.111471222C>A	NCBI36
NG_012337.2:g.13442C>A
NG_012337.3:g.13442C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6277C>A	ENSP00000433202.2:n.314+6277C>A
ENST00000375549.8:c.*318C>A MANE Select	ENSP00000364699.3:n.*318C>A
ENST00000528021.6:c.314+6277C>A	ENSP00000432465.1:n.314+6277C>A
ENST00000375549.7:c.*318C>A	ENSP00000364699.3:n.*318C>A
ENST00000525291.5:c.*318C>A	ENSP00000436669.1:n.*318C>A
ENST00000525987.5:n.319+6277C>A
ENST00000528021.5:c.314+6277C>A	ENSP00000432465.1:n.314+6277C>A
ENST00000528048.5:c.*395C>A	ENSP00000436217.1:n.*395C>A
ENST00000531744.5:c.314+6277C>A	ENSP00000456957.1:n.314+6277C>A
ENST00000532699.1:c.314+6277C>A	ENSP00000456434.1:n.314+6277C>A
ENST00000534010.1:c.145+6277C>A
NM_001276503.1:c.*395C>A	NP_001263432.1:n.*395C>A
NM_001276504.1:c.*318C>A	NP_001263433.1:n.*318C>A
NM_001276506.1:c.*496C>A	NP_001263435.1:n.*496C>A
NM_003002.3:c.*318C>A	NP_002993.1:n.*318C>A
NR_077060.1:n.936C>A
NM_003002.4:c.*318C>A MANE Select	NP_002993.1:n.*318C>A
NM_001276503.2:c.*395C>A	NP_001263432.1:n.*395C>A
NM_001276504.2:c.*318C>A	NP_001263433.1:n.*318C>A
NM_001276506.2:c.*496C>A	NP_001263435.1:n.*496C>A
NR_077060.2:n.887C>A