Canonical Allele Identifier: CA382619381

Gene: SDHD

Linked Data

• dbSNP Id: rs745732631
• gnomAD v2: 11-111965645-A-C
• MyVariant Identifiers: chr11:g.111965645A>C (hg19) ; chr11:g.112094921A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094921A>C , CM000673.2:g.112094921A>C	GRCh38
NC_000011.9:g.111965645A>C , CM000673.1:g.111965645A>C	GRCh37
NC_000011.8:g.111470855A>C	NCBI36
NG_012337.2:g.13075A>C
NG_012337.3:g.13075A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*170A>C	ENSP00000432946.2:n.*170A>C
ENST00000534010.2:c.314+5910A>C	ENSP00000433202.2:n.314+5910A>C
ENST00000375549.8:c.431A>C MANE Select	ENSP00000364699.3:p.Tyr144Ser
ENST00000528021.6:c.314+5910A>C	ENSP00000432465.1:n.314+5910A>C
ENST00000375549.7:c.431A>C	ENSP00000364699.3:p.Tyr144Ser
ENST00000525291.5:c.314A>C	ENSP00000436669.1:p.Tyr105Ser
ENST00000525987.5:n.319+5910A>C
ENST00000526592.5:c.*129A>C	ENSP00000432005.1:n.*129A>C
ENST00000528021.5:c.314+5910A>C	ENSP00000432465.1:n.314+5910A>C
ENST00000528048.5:c.*28A>C	ENSP00000436217.1:n.*28A>C
ENST00000528182.5:c.*28A>C	ENSP00000435475.1:n.*28A>C
ENST00000530923.5:c.475A>C
ENST00000531744.5:c.314+5910A>C	ENSP00000456957.1:n.314+5910A>C
ENST00000532699.1:c.314+5910A>C	ENSP00000456434.1:n.314+5910A>C
ENST00000534010.1:c.145+5910A>C
NM_001276503.1:c.*28A>C	NP_001263432.1:n.*28A>C
NM_001276504.1:c.314A>C	NP_001263433.1:p.Tyr105Ser
NM_001276506.1:c.*129A>C	NP_001263435.1:n.*129A>C
NM_003002.3:c.431A>C	NP_002993.1:p.Tyr144Ser
NR_077060.1:n.569A>C
NM_003002.4:c.431A>C MANE Select	NP_002993.1:p.Tyr144Ser
NM_001276503.2:c.*28A>C	NP_001263432.1:n.*28A>C
NM_001276504.2:c.314A>C	NP_001263433.1:p.Tyr105Ser
NM_001276506.2:c.*129A>C	NP_001263435.1:n.*129A>C
NR_077060.2:n.520A>C