Canonical Allele Identifier: CA2741209279

Gene: SDHD

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112088877_112088878dup , CM000673.2:g.112088877_112088878dup	GRCh38
NC_000011.9:g.111959601_111959602dup , CM000673.1:g.111959601_111959602dup	GRCh37
NC_000011.8:g.111464811_111464812dup	NCBI36
NG_012337.2:g.7031_7032dup
NG_033145.1:g.2921_2922dup
NG_012337.3:g.7031_7032dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.180_181dup	ENSP00000432946.2:p.Ala61GlyfsTer26
ENST00000534010.2:c.180_181dup	ENSP00000433202.2:p.Ala61GlyfsTer26
ENST00000375549.8:c.180_181dup MANE Select	ENSP00000364699.3:p.Ala61GlyfsTer26
ENST00000528021.6:c.180_181dup	ENSP00000432465.1:p.Ala61GlyfsTer26
ENST00000640554.1:c.*252_*253dup	ENSP00000491141.1:n.*252_*253dup
ENST00000375549.7:c.180_181dup	ENSP00000364699.3:p.Ala61GlyfsTer26
ENST00000525291.5:c.63_64dup	ENSP00000436669.1:p.Ala22GlyfsTer26
ENST00000525987.5:n.185_186dup
ENST00000526592.5:c.180_181dup	ENSP00000432005.1:p.Ala61GlyfsTer26
ENST00000528021.5:c.180_181dup	ENSP00000432465.1:p.Ala61GlyfsTer26
ENST00000528048.5:c.169+904_169+905dup	ENSP00000436217.1:n.169+904_169+905dup
ENST00000528182.5:c.180_181dup	ENSP00000435475.1:p.Ala61GlyfsTer26
ENST00000530923.5:c.170_171dup
ENST00000531744.5:c.180_181dup	ENSP00000456957.1:p.Ala61GlyfsTer26
ENST00000532699.1:c.180_181dup	ENSP00000456434.1:p.Ala61GlyfsTer26
ENST00000534010.1:c.11_12dup
ENST00000614349.4:c.180_181dup	ENSP00000480666.1:p.Ala61GlyfsTer26
NM_001276503.1:c.169+904_169+905dup	NP_001263432.1:n.169+904_169+905dup
NM_001276504.1:c.63_64dup	NP_001263433.1:p.Ala22GlyfsTer26
NM_001276506.1:c.180_181dup	NP_001263435.1:p.Ala61GlyfsTer26
NM_003002.3:c.180_181dup	NP_002993.1:p.Ala61GlyfsTer26
NR_077060.1:n.264_265dup
NM_003002.4:c.180_181dup MANE Select	NP_002993.1:p.Ala61GlyfsTer26
NM_001276503.2:c.169+904_169+905dup	NP_001263432.1:n.169+904_169+905dup
NM_001276504.2:c.63_64dup	NP_001263433.1:p.Ala22GlyfsTer26
NM_001276506.2:c.180_181dup	NP_001263435.1:p.Ala61GlyfsTer26
NR_077060.2:n.215_216dup