Canonical Allele Identifier: CA382619183

Gene: SDHD

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*133T>C	ENSP00000432946.2:n.*133T>C
ENST00000534010.2:c.314+5873T>C	ENSP00000433202.2:n.314+5873T>C
ENST00000375549.8:c.394T>C MANE Select	ENSP00000364699.3:p.Ser132Pro
ENST00000528021.6:c.314+5873T>C	ENSP00000432465.1:n.314+5873T>C
ENST00000375549.7:c.394T>C	ENSP00000364699.3:p.Ser132Pro
ENST00000525291.5:c.277T>C	ENSP00000436669.1:p.Ser93Pro
ENST00000525987.5:n.319+5873T>C
ENST00000526592.5:c.*92T>C	ENSP00000432005.1:n.*92T>C
ENST00000528021.5:c.314+5873T>C	ENSP00000432465.1:n.314+5873T>C
ENST00000528048.5:c.249T>C	ENSP00000436217.1:p.Phe83=
ENST00000528182.5:c.387T>C	ENSP00000435475.1:p.Phe129=
ENST00000530923.5:c.438T>C
ENST00000531744.5:c.314+5873T>C	ENSP00000456957.1:n.314+5873T>C
ENST00000532699.1:c.314+5873T>C	ENSP00000456434.1:n.314+5873T>C
ENST00000534010.1:c.145+5873T>C
NM_001276503.1:c.249T>C	NP_001263432.1:p.Phe83=
NM_001276504.1:c.277T>C	NP_001263433.1:p.Ser93Pro
NM_001276506.1:c.*92T>C	NP_001263435.1:n.*92T>C
NM_003002.3:c.394T>C	NP_002993.1:p.Ser132Pro
NR_077060.1:n.532T>C
NM_003002.4:c.394T>C MANE Select	NP_002993.1:p.Ser132Pro
NM_001276503.2:c.249T>C	NP_001263432.1:p.Phe83=
NM_001276504.2:c.277T>C	NP_001263433.1:p.Ser93Pro
NM_001276506.2:c.*92T>C	NP_001263435.1:n.*92T>C
NR_077060.2:n.483T>C