Canonical Allele Identifier: CA382617366

Gene: SDHD

Linked Data

• MyVariant Identifiers: chr11:g.111959698T>G (hg19) ; chr11:g.112088974T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112088974T>G , CM000673.2:g.112088974T>G	GRCh38
NC_000011.9:g.111959698T>G , CM000673.1:g.111959698T>G	GRCh37
NC_000011.8:g.111464908T>G	NCBI36
NG_012337.2:g.7128T>G
NG_033145.1:g.2825A>C
NG_012337.3:g.7128T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.277T>G	ENSP00000432946.2:p.Tyr93Asp
ENST00000534010.2:c.277T>G	ENSP00000433202.2:p.Tyr93Asp
ENST00000375549.8:c.277T>G MANE Select	ENSP00000364699.3:p.Tyr93Asp
ENST00000528021.6:c.277T>G	ENSP00000432465.1:p.Tyr93Asp
ENST00000640554.1:c.*349T>G	ENSP00000491141.1:n.*349T>G
ENST00000375549.7:c.277T>G	ENSP00000364699.3:p.Tyr93Asp
ENST00000525291.5:c.160T>G	ENSP00000436669.1:p.Tyr54Asp
ENST00000525987.5:n.282T>G
ENST00000526592.5:c.277T>G	ENSP00000432005.1:p.Tyr93Asp
ENST00000528021.5:c.277T>G	ENSP00000432465.1:p.Tyr93Asp
ENST00000528048.5:c.169+1001T>G	ENSP00000436217.1:n.169+1001T>G
ENST00000528182.5:c.277T>G	ENSP00000435475.1:p.Tyr93Asp
ENST00000530923.5:c.267T>G
ENST00000531744.5:c.277T>G	ENSP00000456957.1:p.Tyr93Asp
ENST00000532699.1:c.277T>G	ENSP00000456434.1:p.Tyr93Asp
ENST00000534010.1:c.108T>G
ENST00000614349.4:c.277T>G	ENSP00000480666.1:p.Tyr93Asp
NM_001276503.1:c.169+1001T>G	NP_001263432.1:n.169+1001T>G
NM_001276504.1:c.160T>G	NP_001263433.1:p.Tyr54Asp
NM_001276506.1:c.277T>G	NP_001263435.1:p.Tyr93Asp
NM_003002.3:c.277T>G	NP_002993.1:p.Tyr93Asp
NR_077060.1:n.361T>G
NM_003002.4:c.277T>G MANE Select	NP_002993.1:p.Tyr93Asp
NM_001276503.2:c.169+1001T>G	NP_001263432.1:n.169+1001T>G
NM_001276504.2:c.160T>G	NP_001263433.1:p.Tyr54Asp
NM_001276506.2:c.277T>G	NP_001263435.1:p.Tyr93Asp
NR_077060.2:n.312T>G