Canonical Allele Identifier: CA2000553843

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094831A= , CM000673.2:g.112094831A=	GRCh38
NC_000011.9:g.111965555A= , CM000673.1:g.111965555A=	GRCh37
NC_000011.8:g.111470765A=	NCBI36
NG_012337.2:g.12985A=
NG_012337.3:g.12985A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*80A=	ENSP00000432946.2:n.*80A=
ENST00000534010.2:c.314+5820A=	ENSP00000433202.2:n.314+5820A=
ENST00000375549.8:c.341A= MANE Select	ENSP00000364699.3:p.Tyr114=
ENST00000528021.6:c.314+5820A=	ENSP00000432465.1:n.314+5820A=
ENST00000375549.7:c.341A=	ENSP00000364699.3:p.Tyr114=
ENST00000525291.5:c.224A=	ENSP00000436669.1:p.Tyr75=
ENST00000525987.5:n.319+5820A=
ENST00000526592.5:c.*39A=	ENSP00000432005.1:n.*39A=
ENST00000528021.5:c.314+5820A=	ENSP00000432465.1:n.314+5820A=
ENST00000528048.5:c.196A=	ENSP00000436217.1:p.Met66=
ENST00000528182.5:c.334A=	ENSP00000435475.1:p.Met112=
ENST00000530923.5:c.385A=
ENST00000531744.5:c.314+5820A=	ENSP00000456957.1:n.314+5820A=
ENST00000532699.1:c.314+5820A=	ENSP00000456434.1:n.314+5820A=
ENST00000534010.1:c.145+5820A=
NM_001276503.1:c.196A=	NP_001263432.1:p.Met66=
NM_001276504.1:c.224A=	NP_001263433.1:p.Tyr75=
NM_001276506.1:c.*39A=	NP_001263435.1:n.*39A=
NM_003002.3:c.341A=	NP_002993.1:p.Tyr114=
NR_077060.1:n.479A=
NM_003002.4:c.341A= MANE Select	NP_002993.1:p.Tyr114=
NM_001276503.2:c.196A=	NP_001263432.1:p.Met66=
NM_001276504.2:c.224A=	NP_001263433.1:p.Tyr75=
NM_001276506.2:c.*39A=	NP_001263435.1:n.*39A=
NR_077060.2:n.430A=