Canonical Allele Identifier: CA2000560793

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112087874C= , CM000673.2:g.112087874C=	GRCh38
NC_000011.9:g.111958598C= , CM000673.1:g.111958598C=	GRCh37
NC_000011.8:g.111463808C=	NCBI36
NG_012337.2:g.6028C=
NG_033145.1:g.3925G=
NG_012337.3:g.6028C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.70C=	ENSP00000432946.2:p.Pro24=
ENST00000534010.2:c.70C=	ENSP00000433202.2:p.Pro24=
ENST00000375549.8:c.70C= MANE Select	ENSP00000364699.3:p.Pro24=
ENST00000528021.6:c.70C=	ENSP00000432465.1:p.Pro24=
ENST00000640554.1:c.70C=	ENSP00000491141.1:p.Pro24=
ENST00000375549.7:c.70C=	ENSP00000364699.3:p.Pro24=
ENST00000525291.5:c.52+915C=	ENSP00000436669.1:n.52+915C=
ENST00000525987.5:n.75C=
ENST00000526592.5:c.70C=	ENSP00000432005.1:p.Pro24=
ENST00000528021.5:c.70C=	ENSP00000432465.1:p.Pro24=
ENST00000528048.5:c.70C=	ENSP00000436217.1:p.Pro24=
ENST00000528182.5:c.70C=	ENSP00000435475.1:p.Pro24=
ENST00000530923.5:c.60C=
ENST00000531744.5:c.70C=	ENSP00000456957.1:p.Pro24=
ENST00000532699.1:c.70C=	ENSP00000456434.1:p.Pro24=
ENST00000614349.4:c.70C=	ENSP00000480666.1:p.Pro24=
NM_001276503.1:c.70C=	NP_001263432.1:p.Pro24=
NM_001276504.1:c.52+915C=	NP_001263433.1:n.52+915C=
NM_001276506.1:c.70C=	NP_001263435.1:p.Pro24=
NM_003002.3:c.70C=	NP_002993.1:p.Pro24=
NR_077060.1:n.154C=
NM_003002.4:c.70C= MANE Select	NP_002993.1:p.Pro24=
NM_001276503.2:c.70C=	NP_001263432.1:p.Pro24=
NM_001276504.2:c.52+915C=	NP_001263433.1:n.52+915C=
NM_001276506.2:c.70C=	NP_001263435.1:p.Pro24=
NR_077060.2:n.105C=