Canonical Allele Identifier: CA476790457

Gene: SDHD

Linked Data

• MyVariant Identifiers: chr11:g.111959679T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112088955T>C , CM000673.2:g.112088955T>C	GRCh38
NC_000011.9:g.111959679T>C , CM000673.1:g.111959679T>C	GRCh37
NC_000011.8:g.111464889T>C	NCBI36
NG_012337.2:g.7109T>C
NG_033145.1:g.2844A>G
NG_012337.3:g.7109T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.258T>C	ENSP00000432946.2:p.Asn86=
ENST00000534010.2:c.258T>C	ENSP00000433202.2:p.Asn86=
ENST00000375549.8:c.258T>C MANE Select	ENSP00000364699.3:p.Asn86=
ENST00000528021.6:c.258T>C	ENSP00000432465.1:p.Asn86=
ENST00000640554.1:c.*330T>C	ENSP00000491141.1:n.*330T>C
ENST00000375549.7:c.258T>C	ENSP00000364699.3:p.Asn86=
ENST00000525291.5:c.141T>C	ENSP00000436669.1:p.Asn47=
ENST00000525987.5:n.263T>C
ENST00000526592.5:c.258T>C	ENSP00000432005.1:p.Asn86=
ENST00000528021.5:c.258T>C	ENSP00000432465.1:p.Asn86=
ENST00000528048.5:c.169+982T>C	ENSP00000436217.1:n.169+982T>C
ENST00000528182.5:c.258T>C	ENSP00000435475.1:p.Asn86=
ENST00000530923.5:c.248T>C
ENST00000531744.5:c.258T>C	ENSP00000456957.1:p.Asn86=
ENST00000532699.1:c.258T>C	ENSP00000456434.1:p.Asn86=
ENST00000534010.1:c.89T>C
ENST00000614349.4:c.258T>C	ENSP00000480666.1:p.Asn86=
NM_001276503.1:c.169+982T>C	NP_001263432.1:n.169+982T>C
NM_001276504.1:c.141T>C	NP_001263433.1:p.Asn47=
NM_001276506.1:c.258T>C	NP_001263435.1:p.Asn86=
NM_003002.3:c.258T>C	NP_002993.1:p.Asn86=
NR_077060.1:n.342T>C
NM_003002.4:c.258T>C MANE Select	NP_002993.1:p.Asn86=
NM_001276503.2:c.169+982T>C	NP_001263432.1:n.169+982T>C
NM_001276504.2:c.141T>C	NP_001263433.1:p.Asn47=
NM_001276506.2:c.258T>C	NP_001263435.1:p.Asn86=
NR_077060.2:n.293T>C