Canonical Allele Identifier: CA2000559536

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086883A= , CM000673.2:g.112086883A=	GRCh38
NC_000011.9:g.111957607A= , CM000673.1:g.111957607A=	GRCh37
NC_000011.8:g.111462817A=	NCBI36
NG_012337.2:g.5037A=
NG_033145.1:g.4916T=
NG_012337.3:g.5037A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.-25A=	ENSP00000432946.2:n.-25A=
ENST00000534010.2:c.-25A=	ENSP00000433202.2:n.-25A=
ENST00000375549.8:c.-25A= MANE Select	ENSP00000364699.3:n.-25A=
ENST00000528021.6:c.-25A=	ENSP00000432465.1:n.-25A=
ENST00000640554.1:c.-25A=	ENSP00000491141.1:n.-25A=
ENST00000375549.7:c.-25A=	ENSP00000364699.3:n.-25A=
ENST00000528021.5:c.-25A=	ENSP00000432465.1:n.-25A=
ENST00000528048.5:c.-25A=	ENSP00000436217.1:n.-25A=
ENST00000528182.5:c.-25A=	ENSP00000435475.1:n.-25A=
ENST00000614349.4:c.-25A=	ENSP00000480666.1:n.-25A=
NM_001276503.1:c.-25A=	NP_001263432.1:n.-25A=
NM_001276504.1:c.-25A=	NP_001263433.1:n.-25A=
NM_001276506.1:c.-25A=	NP_001263435.1:n.-25A=
NM_003002.3:c.-25A=	NP_002993.1:n.-25A=
NR_077060.1:n.60A=
NM_003002.4:c.-25A= MANE Select	NP_002993.1:n.-25A=
NM_001276503.2:c.-25A=	NP_001263432.1:n.-25A=
NM_001276504.2:c.-25A=	NP_001263433.1:n.-25A=
NM_001276506.2:c.-25A=	NP_001263435.1:n.-25A=
NR_077060.2:n.11A=