Canonical Allele Identifier: CA382619181

Gene: SDHD

Linked Data

• MyVariant Identifiers: chr11:g.111965608T>A (hg19) ; chr11:g.112094884T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094884T>A , CM000673.2:g.112094884T>A	GRCh38
NC_000011.9:g.111965608T>A , CM000673.1:g.111965608T>A	GRCh37
NC_000011.8:g.111470818T>A	NCBI36
NG_012337.2:g.13038T>A
NG_012337.3:g.13038T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*133T>A	ENSP00000432946.2:n.*133T>A
ENST00000534010.2:c.314+5873T>A	ENSP00000433202.2:n.314+5873T>A
ENST00000375549.8:c.394T>A MANE Select	ENSP00000364699.3:p.Ser132Thr
ENST00000528021.6:c.314+5873T>A	ENSP00000432465.1:n.314+5873T>A
ENST00000375549.7:c.394T>A	ENSP00000364699.3:p.Ser132Thr
ENST00000525291.5:c.277T>A	ENSP00000436669.1:p.Ser93Thr
ENST00000525987.5:n.319+5873T>A
ENST00000526592.5:c.*92T>A	ENSP00000432005.1:n.*92T>A
ENST00000528021.5:c.314+5873T>A	ENSP00000432465.1:n.314+5873T>A
ENST00000528048.5:c.249T>A	ENSP00000436217.1:p.Phe83Leu
ENST00000528182.5:c.387T>A	ENSP00000435475.1:p.Phe129Leu
ENST00000530923.5:c.438T>A
ENST00000531744.5:c.314+5873T>A	ENSP00000456957.1:n.314+5873T>A
ENST00000532699.1:c.314+5873T>A	ENSP00000456434.1:n.314+5873T>A
ENST00000534010.1:c.145+5873T>A
NM_001276503.1:c.249T>A	NP_001263432.1:p.Phe83Leu
NM_001276504.1:c.277T>A	NP_001263433.1:p.Ser93Thr
NM_001276506.1:c.*92T>A	NP_001263435.1:n.*92T>A
NM_003002.3:c.394T>A	NP_002993.1:p.Ser132Thr
NR_077060.1:n.532T>A
NM_003002.4:c.394T>A MANE Select	NP_002993.1:p.Ser132Thr
NM_001276503.2:c.249T>A	NP_001263432.1:p.Phe83Leu
NM_001276504.2:c.277T>A	NP_001263433.1:p.Ser93Thr
NM_001276506.2:c.*92T>A	NP_001263435.1:n.*92T>A
NR_077060.2:n.483T>A