Canonical Allele Identifier: CA2000554042

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094906T= , CM000673.2:g.112094906T=	GRCh38
NC_000011.9:g.111965630T= , CM000673.1:g.111965630T=	GRCh37
NC_000011.8:g.111470840T=	NCBI36
NG_012337.2:g.13060T=
NG_012337.3:g.13060T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*155T=	ENSP00000432946.2:n.*155T=
ENST00000534010.2:c.314+5895T=	ENSP00000433202.2:n.314+5895T=
ENST00000375549.8:c.416T= MANE Select	ENSP00000364699.3:p.Leu139=
ENST00000528021.6:c.314+5895T=	ENSP00000432465.1:n.314+5895T=
ENST00000375549.7:c.416T=	ENSP00000364699.3:p.Leu139=
ENST00000525291.5:c.299T=	ENSP00000436669.1:p.Leu100=
ENST00000525987.5:n.319+5895T=
ENST00000526592.5:c.*114T=	ENSP00000432005.1:n.*114T=
ENST00000528021.5:c.314+5895T=	ENSP00000432465.1:n.314+5895T=
ENST00000528048.5:c.*13T=	ENSP00000436217.1:n.*13T=
ENST00000528182.5:c.*13T=	ENSP00000435475.1:n.*13T=
ENST00000530923.5:c.460T=
ENST00000531744.5:c.314+5895T=	ENSP00000456957.1:n.314+5895T=
ENST00000532699.1:c.314+5895T=	ENSP00000456434.1:n.314+5895T=
ENST00000534010.1:c.145+5895T=
NM_001276503.1:c.*13T=	NP_001263432.1:n.*13T=
NM_001276504.1:c.299T=	NP_001263433.1:p.Leu100=
NM_001276506.1:c.*114T=	NP_001263435.1:n.*114T=
NM_003002.3:c.416T=	NP_002993.1:p.Leu139=
NR_077060.1:n.554T=
NM_003002.4:c.416T= MANE Select	NP_002993.1:p.Leu139=
NM_001276503.2:c.*13T=	NP_001263432.1:n.*13T=
NM_001276504.2:c.299T=	NP_001263433.1:p.Leu100=
NM_001276506.2:c.*114T=	NP_001263435.1:n.*114T=
NR_077060.2:n.505T=