Canonical Allele Identifier: CA382619511

Gene: SDHD

Linked Data

• MyVariant Identifiers: chr11:g.111965668G>C (hg19) ; chr11:g.112094944G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094944G>C , CM000673.2:g.112094944G>C	GRCh38
NC_000011.9:g.111965668G>C , CM000673.1:g.111965668G>C	GRCh37
NC_000011.8:g.111470878G>C	NCBI36
NG_012337.2:g.13098G>C
NG_012337.3:g.13098G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*193G>C	ENSP00000432946.2:n.*193G>C
ENST00000534010.2:c.314+5933G>C	ENSP00000433202.2:n.314+5933G>C
ENST00000375549.8:c.454G>C MANE Select	ENSP00000364699.3:p.Ala152Pro
ENST00000528021.6:c.314+5933G>C	ENSP00000432465.1:n.314+5933G>C
ENST00000375549.7:c.454G>C	ENSP00000364699.3:p.Ala152Pro
ENST00000525291.5:c.337G>C	ENSP00000436669.1:p.Ala113Pro
ENST00000525987.5:n.319+5933G>C
ENST00000526592.5:c.*152G>C	ENSP00000432005.1:n.*152G>C
ENST00000528021.5:c.314+5933G>C	ENSP00000432465.1:n.314+5933G>C
ENST00000528048.5:c.*51G>C	ENSP00000436217.1:n.*51G>C
ENST00000528182.5:c.*51G>C	ENSP00000435475.1:n.*51G>C
ENST00000530923.5:c.498G>C
ENST00000531744.5:c.314+5933G>C	ENSP00000456957.1:n.314+5933G>C
ENST00000532699.1:c.314+5933G>C	ENSP00000456434.1:n.314+5933G>C
ENST00000534010.1:c.145+5933G>C
NM_001276503.1:c.*51G>C	NP_001263432.1:n.*51G>C
NM_001276504.1:c.337G>C	NP_001263433.1:p.Ala113Pro
NM_001276506.1:c.*152G>C	NP_001263435.1:n.*152G>C
NM_003002.3:c.454G>C	NP_002993.1:p.Ala152Pro
NR_077060.1:n.592G>C
NM_003002.4:c.454G>C MANE Select	NP_002993.1:p.Ala152Pro
NM_001276503.2:c.*51G>C	NP_001263432.1:n.*51G>C
NM_001276504.2:c.337G>C	NP_001263433.1:p.Ala113Pro
NM_001276506.2:c.*152G>C	NP_001263435.1:n.*152G>C
NR_077060.2:n.543G>C