Canonical Allele Identifier: CA2000553745

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094806G= , CM000673.2:g.112094806G=	GRCh38
NC_000011.9:g.111965530G= , CM000673.1:g.111965530G=	GRCh37
NC_000011.8:g.111470740G=	NCBI36
NG_012337.2:g.12960G=
NG_012337.3:g.12960G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.*55G=	ENSP00000432946.2:n.*55G=
ENST00000534010.2:c.314+5795G=	ENSP00000433202.2:n.314+5795G=
ENST00000375549.8:c.316G= MANE Select	ENSP00000364699.3:p.Gly106=
ENST00000528021.6:c.314+5795G=	ENSP00000432465.1:n.314+5795G=
ENST00000375549.7:c.316G=	ENSP00000364699.3:p.Gly106=
ENST00000525291.5:c.199G=	ENSP00000436669.1:p.Gly67=
ENST00000525987.5:n.319+5795G=
ENST00000526592.5:c.*14G=	ENSP00000432005.1:n.*14G=
ENST00000528021.5:c.314+5795G=	ENSP00000432465.1:n.314+5795G=
ENST00000528048.5:c.171G=	ENSP00000436217.1:p.Trp57=
ENST00000528182.5:c.309G=	ENSP00000435475.1:p.Gly103=
ENST00000530923.5:c.360G=
ENST00000531744.5:c.314+5795G=	ENSP00000456957.1:n.314+5795G=
ENST00000532699.1:c.314+5795G=	ENSP00000456434.1:n.314+5795G=
ENST00000534010.1:c.145+5795G=
NM_001276503.1:c.171G=	NP_001263432.1:p.Trp57=
NM_001276504.1:c.199G=	NP_001263433.1:p.Gly67=
NM_001276506.1:c.*14G=	NP_001263435.1:n.*14G=
NM_003002.3:c.316G=	NP_002993.1:p.Gly106=
NR_077060.1:n.454G=
NM_003002.4:c.316G= MANE Select	NP_002993.1:p.Gly106=
NM_001276503.2:c.171G=	NP_001263432.1:p.Trp57=
NM_001276504.2:c.199G=	NP_001263433.1:p.Gly67=
NM_001276506.2:c.*14G=	NP_001263435.1:n.*14G=
NR_077060.2:n.405G=