Canonical Allele Identifier: CA2000562022

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112088971G= , CM000673.2:g.112088971G=	GRCh38
NC_000011.9:g.111959695G= , CM000673.1:g.111959695G=	GRCh37
NC_000011.8:g.111464905G=	NCBI36
NG_012337.2:g.7125G=
NG_033145.1:g.2828C=
NG_012337.3:g.7125G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.274G=	ENSP00000432946.2:p.Asp92=
ENST00000534010.2:c.274G=	ENSP00000433202.2:p.Asp92=
ENST00000375549.8:c.274G= MANE Select	ENSP00000364699.3:p.Asp92=
ENST00000528021.6:c.274G=	ENSP00000432465.1:p.Asp92=
ENST00000640554.1:c.*346G=	ENSP00000491141.1:n.*346G=
ENST00000375549.7:c.274G=	ENSP00000364699.3:p.Asp92=
ENST00000525291.5:c.157G=	ENSP00000436669.1:p.Asp53=
ENST00000525987.5:n.279G=
ENST00000526592.5:c.274G=	ENSP00000432005.1:p.Asp92=
ENST00000528021.5:c.274G=	ENSP00000432465.1:p.Asp92=
ENST00000528048.5:c.169+998G=	ENSP00000436217.1:n.169+998G=
ENST00000528182.5:c.274G=	ENSP00000435475.1:p.Asp92=
ENST00000530923.5:c.264G=
ENST00000531744.5:c.274G=	ENSP00000456957.1:p.Asp92=
ENST00000532699.1:c.274G=	ENSP00000456434.1:p.Asp92=
ENST00000534010.1:c.105G=
ENST00000614349.4:c.274G=	ENSP00000480666.1:p.Asp92=
NM_001276503.1:c.169+998G=	NP_001263432.1:n.169+998G=
NM_001276504.1:c.157G=	NP_001263433.1:p.Asp53=
NM_001276506.1:c.274G=	NP_001263435.1:p.Asp92=
NM_003002.3:c.274G=	NP_002993.1:p.Asp92=
NR_077060.1:n.358G=
NM_003002.4:c.274G= MANE Select	NP_002993.1:p.Asp92=
NM_001276503.2:c.169+998G=	NP_001263432.1:n.169+998G=
NM_001276504.2:c.157G=	NP_001263433.1:p.Asp53=
NM_001276506.2:c.274G=	NP_001263435.1:p.Asp92=
NR_077060.2:n.309G=