Canonical Allele Identifier: CA382619027

Gene: SDHD

Linked Data

• ClinVar Variation Id: 957437
• ClinVar RCV Id: RCV002241444 ; RCV003294101
• dbSNP Id: rs1865811210
• gnomAD v4: 11-112094861-C-T
• MyVariant Identifiers: chr11:g.111965585C>T (hg19) ; chr11:g.112094861C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094861C>T , CM000673.2:g.112094861C>T	GRCh38
NC_000011.9:g.111965585C>T , CM000673.1:g.111965585C>T	GRCh37
NC_000011.8:g.111470795C>T	NCBI36
NG_012337.2:g.13015C>T
NG_012337.3:g.13015C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*110C>T	ENSP00000432946.2:n.*110C>T
ENST00000534010.2:c.314+5850C>T	ENSP00000433202.2:n.314+5850C>T
ENST00000375549.8:c.371C>T MANE Select	ENSP00000364699.3:p.Ala124Val
ENST00000528021.6:c.314+5850C>T	ENSP00000432465.1:n.314+5850C>T
ENST00000375549.7:c.371C>T	ENSP00000364699.3:p.Ala124Val
ENST00000525291.5:c.254C>T	ENSP00000436669.1:p.Ala85Val
ENST00000525987.5:n.319+5850C>T
ENST00000526592.5:c.*69C>T	ENSP00000432005.1:n.*69C>T
ENST00000528021.5:c.314+5850C>T	ENSP00000432465.1:n.314+5850C>T
ENST00000528048.5:c.226C>T	ENSP00000436217.1:p.Pro76Ser
ENST00000528182.5:c.364C>T	ENSP00000435475.1:p.Pro122Ser
ENST00000530923.5:c.415C>T
ENST00000531744.5:c.314+5850C>T	ENSP00000456957.1:n.314+5850C>T
ENST00000532699.1:c.314+5850C>T	ENSP00000456434.1:n.314+5850C>T
ENST00000534010.1:c.145+5850C>T
NM_001276503.1:c.226C>T	NP_001263432.1:p.Pro76Ser
NM_001276504.1:c.254C>T	NP_001263433.1:p.Ala85Val
NM_001276506.1:c.*69C>T	NP_001263435.1:n.*69C>T
NM_003002.3:c.371C>T	NP_002993.1:p.Ala124Val
NR_077060.1:n.509C>T
NM_003002.4:c.371C>T MANE Select	NP_002993.1:p.Ala124Val
NM_001276503.2:c.226C>T	NP_001263432.1:p.Pro76Ser
NM_001276504.2:c.254C>T	NP_001263433.1:p.Ala85Val
NM_001276506.2:c.*69C>T	NP_001263435.1:n.*69C>T
NR_077060.2:n.460C>T