Canonical Allele Identifier: CA2000559544

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086885G= , CM000673.2:g.112086885G=	GRCh38
NC_000011.9:g.111957609G= , CM000673.1:g.111957609G=	GRCh37
NC_000011.8:g.111462819G=	NCBI36
NG_012337.2:g.5039G=
NG_033145.1:g.4914C=
NG_012337.3:g.5039G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.-23G=	ENSP00000432946.2:n.-23G=
ENST00000534010.2:c.-23G=	ENSP00000433202.2:n.-23G=
ENST00000375549.8:c.-23G= MANE Select	ENSP00000364699.3:n.-23G=
ENST00000528021.6:c.-23G=	ENSP00000432465.1:n.-23G=
ENST00000640554.1:c.-23G=	ENSP00000491141.1:n.-23G=
ENST00000375549.7:c.-23G=	ENSP00000364699.3:n.-23G=
ENST00000528021.5:c.-23G=	ENSP00000432465.1:n.-23G=
ENST00000528048.5:c.-23G=	ENSP00000436217.1:n.-23G=
ENST00000528182.5:c.-23G=	ENSP00000435475.1:n.-23G=
ENST00000614349.4:c.-23G=	ENSP00000480666.1:n.-23G=
NM_001276503.1:c.-23G=	NP_001263432.1:n.-23G=
NM_001276504.1:c.-23G=	NP_001263433.1:n.-23G=
NM_001276506.1:c.-23G=	NP_001263435.1:n.-23G=
NM_003002.3:c.-23G=	NP_002993.1:n.-23G=
NR_077060.1:n.62G=
NM_003002.4:c.-23G= MANE Select	NP_002993.1:n.-23G=
NM_001276503.2:c.-23G=	NP_001263432.1:n.-23G=
NM_001276504.2:c.-23G=	NP_001263433.1:n.-23G=
NM_001276506.2:c.-23G=	NP_001263435.1:n.-23G=
NR_077060.2:n.13G=