Canonical Allele Identifier: CA2615987198

Gene: SDHD

Linked Data

• gnomAD v4: 11-112095144-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095144G>T , CM000673.2:g.112095144G>T	GRCh38
NC_000011.9:g.111965868G>T , CM000673.1:g.111965868G>T	GRCh37
NC_000011.8:g.111471078G>T	NCBI36
NG_012337.2:g.13298G>T
NG_012337.3:g.13298G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*393G>T	ENSP00000432946.2:n.*393G>T
ENST00000534010.2:c.314+6133G>T	ENSP00000433202.2:n.314+6133G>T
ENST00000375549.8:c.*174G>T MANE Select	ENSP00000364699.3:n.*174G>T
ENST00000528021.6:c.314+6133G>T	ENSP00000432465.1:n.314+6133G>T
ENST00000375549.7:c.*174G>T	ENSP00000364699.3:n.*174G>T
ENST00000525291.5:c.*174G>T	ENSP00000436669.1:n.*174G>T
ENST00000525987.5:n.319+6133G>T
ENST00000526592.5:c.*352G>T	ENSP00000432005.1:n.*352G>T
ENST00000528021.5:c.314+6133G>T	ENSP00000432465.1:n.314+6133G>T
ENST00000528048.5:c.*251G>T	ENSP00000436217.1:n.*251G>T
ENST00000528182.5:c.*251G>T	ENSP00000435475.1:n.*251G>T
ENST00000530923.5:c.698G>T
ENST00000531744.5:c.314+6133G>T	ENSP00000456957.1:n.314+6133G>T
ENST00000532699.1:c.314+6133G>T	ENSP00000456434.1:n.314+6133G>T
ENST00000534010.1:c.145+6133G>T
NM_001276503.1:c.*251G>T	NP_001263432.1:n.*251G>T
NM_001276504.1:c.*174G>T	NP_001263433.1:n.*174G>T
NM_001276506.1:c.*352G>T	NP_001263435.1:n.*352G>T
NM_003002.3:c.*174G>T	NP_002993.1:n.*174G>T
NR_077060.1:n.792G>T
NM_003002.4:c.*174G>T MANE Select	NP_002993.1:n.*174G>T
NM_001276503.2:c.*251G>T	NP_001263432.1:n.*251G>T
NM_001276504.2:c.*174G>T	NP_001263433.1:n.*174G>T
NM_001276506.2:c.*352G>T	NP_001263435.1:n.*352G>T
NR_077060.2:n.743G>T