Canonical Allele Identifier: CA2000554063

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094918A= , CM000673.2:g.112094918A=	GRCh38
NC_000011.9:g.111965642A= , CM000673.1:g.111965642A=	GRCh37
NC_000011.8:g.111470852A=	NCBI36
NG_012337.2:g.13072A=
NG_012337.3:g.13072A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*167A=	ENSP00000432946.2:n.*167A=
ENST00000534010.2:c.314+5907A=	ENSP00000433202.2:n.314+5907A=
ENST00000375549.8:c.428A= MANE Select	ENSP00000364699.3:p.Asn143=
ENST00000528021.6:c.314+5907A=	ENSP00000432465.1:n.314+5907A=
ENST00000375549.7:c.428A=	ENSP00000364699.3:p.Asn143=
ENST00000525291.5:c.311A=	ENSP00000436669.1:p.Asn104=
ENST00000525987.5:n.319+5907A=
ENST00000526592.5:c.*126A=	ENSP00000432005.1:n.*126A=
ENST00000528021.5:c.314+5907A=	ENSP00000432465.1:n.314+5907A=
ENST00000528048.5:c.*25A=	ENSP00000436217.1:n.*25A=
ENST00000528182.5:c.*25A=	ENSP00000435475.1:n.*25A=
ENST00000530923.5:c.472A=
ENST00000531744.5:c.314+5907A=	ENSP00000456957.1:n.314+5907A=
ENST00000532699.1:c.314+5907A=	ENSP00000456434.1:n.314+5907A=
ENST00000534010.1:c.145+5907A=
NM_001276503.1:c.*25A=	NP_001263432.1:n.*25A=
NM_001276504.1:c.311A=	NP_001263433.1:p.Asn104=
NM_001276506.1:c.*126A=	NP_001263435.1:n.*126A=
NM_003002.3:c.428A=	NP_002993.1:p.Asn143=
NR_077060.1:n.566A=
NM_003002.4:c.428A= MANE Select	NP_002993.1:p.Asn143=
NM_001276503.2:c.*25A=	NP_001263432.1:n.*25A=
NM_001276504.2:c.311A=	NP_001263433.1:p.Asn104=
NM_001276506.2:c.*126A=	NP_001263435.1:n.*126A=
NR_077060.2:n.517A=