Canonical Allele Identifier: CA2000554290

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095063A= , CM000673.2:g.112095063A=	GRCh38
NC_000011.9:g.111965787A= , CM000673.1:g.111965787A=	GRCh37
NC_000011.8:g.111470997A=	NCBI36
NG_012337.2:g.13217A=
NG_012337.3:g.13217A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*312A=	ENSP00000432946.2:n.*312A=
ENST00000534010.2:c.314+6052A=	ENSP00000433202.2:n.314+6052A=
ENST00000375549.8:c.*93A= MANE Select	ENSP00000364699.3:n.*93A=
ENST00000528021.6:c.314+6052A=	ENSP00000432465.1:n.314+6052A=
ENST00000375549.7:c.*93A=	ENSP00000364699.3:n.*93A=
ENST00000525291.5:c.*93A=	ENSP00000436669.1:n.*93A=
ENST00000525987.5:n.319+6052A=
ENST00000526592.5:c.*271A=	ENSP00000432005.1:n.*271A=
ENST00000528021.5:c.314+6052A=	ENSP00000432465.1:n.314+6052A=
ENST00000528048.5:c.*170A=	ENSP00000436217.1:n.*170A=
ENST00000528182.5:c.*170A=	ENSP00000435475.1:n.*170A=
ENST00000530923.5:c.617A=
ENST00000531744.5:c.314+6052A=	ENSP00000456957.1:n.314+6052A=
ENST00000532699.1:c.314+6052A=	ENSP00000456434.1:n.314+6052A=
ENST00000534010.1:c.145+6052A=
NM_001276503.1:c.*170A=	NP_001263432.1:n.*170A=
NM_001276504.1:c.*93A=	NP_001263433.1:n.*93A=
NM_001276506.1:c.*271A=	NP_001263435.1:n.*271A=
NM_003002.3:c.*93A=	NP_002993.1:n.*93A=
NR_077060.1:n.711A=
NM_003002.4:c.*93A= MANE Select	NP_002993.1:n.*93A=
NM_001276503.2:c.*170A=	NP_001263432.1:n.*170A=
NM_001276504.2:c.*93A=	NP_001263433.1:n.*93A=
NM_001276506.2:c.*271A=	NP_001263435.1:n.*271A=
NR_077060.2:n.662A=