Canonical Allele Identifier: CA2000553849

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094832T= , CM000673.2:g.112094832T=	GRCh38
NC_000011.9:g.111965556T= , CM000673.1:g.111965556T=	GRCh37
NC_000011.8:g.111470766T=	NCBI36
NG_012337.2:g.12986T=
NG_012337.3:g.12986T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*81T=	ENSP00000432946.2:n.*81T=
ENST00000534010.2:c.314+5821T=	ENSP00000433202.2:n.314+5821T=
ENST00000375549.8:c.342T= MANE Select	ENSP00000364699.3:p.Tyr114=
ENST00000528021.6:c.314+5821T=	ENSP00000432465.1:n.314+5821T=
ENST00000375549.7:c.342T=	ENSP00000364699.3:p.Tyr114=
ENST00000525291.5:c.225T=	ENSP00000436669.1:p.Tyr75=
ENST00000525987.5:n.319+5821T=
ENST00000526592.5:c.*40T=	ENSP00000432005.1:n.*40T=
ENST00000528021.5:c.314+5821T=	ENSP00000432465.1:n.314+5821T=
ENST00000528048.5:c.197T=	ENSP00000436217.1:p.Met66=
ENST00000528182.5:c.335T=	ENSP00000435475.1:p.Met112=
ENST00000530923.5:c.386T=
ENST00000531744.5:c.314+5821T=	ENSP00000456957.1:n.314+5821T=
ENST00000532699.1:c.314+5821T=	ENSP00000456434.1:n.314+5821T=
ENST00000534010.1:c.145+5821T=
NM_001276503.1:c.197T=	NP_001263432.1:p.Met66=
NM_001276504.1:c.225T=	NP_001263433.1:p.Tyr75=
NM_001276506.1:c.*40T=	NP_001263435.1:n.*40T=
NM_003002.3:c.342T=	NP_002993.1:p.Tyr114=
NR_077060.1:n.480T=
NM_003002.4:c.342T= MANE Select	NP_002993.1:p.Tyr114=
NM_001276503.2:c.197T=	NP_001263432.1:p.Met66=
NM_001276504.2:c.225T=	NP_001263433.1:p.Tyr75=
NM_001276506.2:c.*40T=	NP_001263435.1:n.*40T=
NR_077060.2:n.431T=