Canonical Allele Identifier: CA382619148

Gene: SDHD

Linked Data

• ClinVar Variation Id: 1513960
• ClinVar RCV Id: RCV002026438
• dbSNP Id: rs1312671864
• MyVariant Identifiers: chr11:g.111965602G>T (hg19) ; chr11:g.112094878G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094878G>T , CM000673.2:g.112094878G>T	GRCh38
NC_000011.9:g.111965602G>T , CM000673.1:g.111965602G>T	GRCh37
NC_000011.8:g.111470812G>T	NCBI36
NG_012337.2:g.13032G>T
NG_012337.3:g.13032G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*127G>T	ENSP00000432946.2:n.*127G>T
ENST00000534010.2:c.314+5867G>T	ENSP00000433202.2:n.314+5867G>T
ENST00000375549.8:c.388G>T MANE Select	ENSP00000364699.3:p.Ala130Ser
ENST00000528021.6:c.314+5867G>T	ENSP00000432465.1:n.314+5867G>T
ENST00000375549.7:c.388G>T	ENSP00000364699.3:p.Ala130Ser
ENST00000525291.5:c.271G>T	ENSP00000436669.1:p.Ala91Ser
ENST00000525987.5:n.319+5867G>T
ENST00000526592.5:c.*86G>T	ENSP00000432005.1:n.*86G>T
ENST00000528021.5:c.314+5867G>T	ENSP00000432465.1:n.314+5867G>T
ENST00000528048.5:c.243G>T	ENSP00000436217.1:p.Trp81Cys
ENST00000528182.5:c.381G>T	ENSP00000435475.1:p.Trp127Cys
ENST00000530923.5:c.432G>T
ENST00000531744.5:c.314+5867G>T	ENSP00000456957.1:n.314+5867G>T
ENST00000532699.1:c.314+5867G>T	ENSP00000456434.1:n.314+5867G>T
ENST00000534010.1:c.145+5867G>T
NM_001276503.1:c.243G>T	NP_001263432.1:p.Trp81Cys
NM_001276504.1:c.271G>T	NP_001263433.1:p.Ala91Ser
NM_001276506.1:c.*86G>T	NP_001263435.1:n.*86G>T
NM_003002.3:c.388G>T	NP_002993.1:p.Ala130Ser
NR_077060.1:n.526G>T
NM_003002.4:c.388G>T MANE Select	NP_002993.1:p.Ala130Ser
NM_001276503.2:c.243G>T	NP_001263432.1:p.Trp81Cys
NM_001276504.2:c.271G>T	NP_001263433.1:p.Ala91Ser
NM_001276506.2:c.*86G>T	NP_001263435.1:n.*86G>T
NR_077060.2:n.477G>T