Canonical Allele Identifier: CA421409263

Gene: SDHC

Linked Data

• gnomAD v4: 1-161340654-A-T
• MyVariant Identifiers: chr1:g.161310444A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161340654A>T , CM000663.2:g.161340654A>T	GRCh38
NC_000001.10:g.161310444A>T , CM000663.1:g.161310444A>T	GRCh37
NC_000001.9:g.159577068A>T	NCBI36
NG_012767.1:g.31279A>T , LRG_317:g.31279A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000470743.5:c.*241A>T	ENSP00000482902.2:n.*241A>T
ENST00000367975.7:c.240A>T MANE Select	ENSP00000356953.3:p.Ala80=
ENST00000342751.8:c.240A>T	ENSP00000356952.3:p.Ala80=
ENST00000367975.6:c.240A>T	ENSP00000356953.2:p.Ala80=
ENST00000392169.6:c.81A>T	ENSP00000376009.2:p.Ala27=
ENST00000432287.6:c.138A>T	ENSP00000390558.2:p.Ala46=
ENST00000470743.4:c.338A>T
ENST00000504963.5:c.*63A>T	ENSP00000423929.1:n.*63A>T
ENST00000513009.5:c.138A>T	ENSP00000423260.1:p.Ala46=
NM_001035511.1:c.240A>T	NP_001030588.1:p.Ala80=
NM_001035512.1:c.138A>T	NP_001030589.1:p.Ala46=
NM_001035513.1:c.81A>T	NP_001030590.1:p.Ala27=
NM_001278172.1:c.138A>T	NP_001265101.1:p.Ala46=
NM_003001.3:c.240A>T , LRG_317t1:c.240A>T	NP_002992.1:p.Ala80=
NR_103459.1:n.297A>T
NM_001035511.2:c.240A>T	NP_001030588.1:p.Ala80=
NM_001035512.2:c.138A>T	NP_001030589.1:p.Ala46=
NM_001035513.2:c.81A>T	NP_001030590.1:p.Ala27=
NM_001278172.2:c.138A>T	NP_001265101.1:p.Ala46=
NM_003001.5:c.240A>T MANE Select	NP_002992.1:p.Ala80=
NR_103459.2:n.292A>T