Canonical Allele Identifier: CA382619236

Gene: SDHD

Linked Data

• MyVariant Identifiers: chr11:g.111965617A>C (hg19) ; chr11:g.112094893A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112094893A>C , CM000673.2:g.112094893A>C	GRCh38
NC_000011.9:g.111965617A>C , CM000673.1:g.111965617A>C	GRCh37
NC_000011.8:g.111470827A>C	NCBI36
NG_012337.2:g.13047A>C
NG_012337.3:g.13047A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.*142A>C	ENSP00000432946.2:n.*142A>C
ENST00000534010.2:c.314+5882A>C	ENSP00000433202.2:n.314+5882A>C
ENST00000375549.8:c.403A>C MANE Select	ENSP00000364699.3:p.Thr135Pro
ENST00000528021.6:c.314+5882A>C	ENSP00000432465.1:n.314+5882A>C
ENST00000375549.7:c.403A>C	ENSP00000364699.3:p.Thr135Pro
ENST00000525291.5:c.286A>C	ENSP00000436669.1:p.Thr96Pro
ENST00000525987.5:n.319+5882A>C
ENST00000526592.5:c.*101A>C	ENSP00000432005.1:n.*101A>C
ENST00000528021.5:c.314+5882A>C	ENSP00000432465.1:n.314+5882A>C
ENST00000528048.5:c.258A>C	ENSP00000436217.1:p.Ter86Tyr
ENST00000528182.5:c.396A>C	ENSP00000435475.1:p.Ter132Tyr
ENST00000530923.5:c.447A>C
ENST00000531744.5:c.314+5882A>C	ENSP00000456957.1:n.314+5882A>C
ENST00000532699.1:c.314+5882A>C	ENSP00000456434.1:n.314+5882A>C
ENST00000534010.1:c.145+5882A>C
NM_001276503.1:c.258A>C	NP_001263432.1:p.Ter86Tyr
NM_001276504.1:c.286A>C	NP_001263433.1:p.Thr96Pro
NM_001276506.1:c.*101A>C	NP_001263435.1:n.*101A>C
NM_003002.3:c.403A>C	NP_002993.1:p.Thr135Pro
NR_077060.1:n.541A>C
NM_003002.4:c.403A>C MANE Select	NP_002993.1:p.Thr135Pro
NM_001276503.2:c.258A>C	NP_001263432.1:p.Ter86Tyr
NM_001276504.2:c.286A>C	NP_001263433.1:p.Thr96Pro
NM_001276506.2:c.*101A>C	NP_001263435.1:n.*101A>C
NR_077060.2:n.492A>C