Canonical Allele Identifier: CA2648774831

Gene: SDHC

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161323536_161323537del , CM000663.2:g.161323536_161323537del	GRCh38
NC_000001.10:g.161293326_161293327del , CM000663.1:g.161293326_161293327del	GRCh37
NC_000001.9:g.159559950_159559951del	NCBI36
NG_012767.1:g.14161_14162del , LRG_317:g.14161_14162del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.21-78_21-77del	ENSP00000482902.2:n.21-78_21-77del
ENST00000367975.7:c.21-78_21-77del MANE Select	ENSP00000356953.3:n.21-78_21-77del
ENST00000342751.8:c.21-78_21-77del	ENSP00000356952.3:n.21-78_21-77del
ENST00000367975.6:c.21-78_21-77del	ENSP00000356953.2:n.21-78_21-77del
ENST00000392169.6:c.20+9111_20+9112del	ENSP00000376009.2:n.20+9111_20+9112del
ENST00000432287.6:c.21-78_21-77del	ENSP00000390558.2:n.21-78_21-77del
ENST00000504963.5:c.21-78_21-77del	ENSP00000423929.1:n.21-78_21-77del
ENST00000513009.5:c.21-78_21-77del	ENSP00000423260.1:n.21-78_21-77del
ENST00000515731.1:n.495-78_495-77del
NM_001035511.1:c.21-78_21-77del	NP_001030588.1:n.21-78_21-77del
NM_001035512.1:c.21-78_21-77del	NP_001030589.1:n.21-78_21-77del
NM_001035513.1:c.20+9111_20+9112del	NP_001030590.1:n.20+9111_20+9112del
NM_001278172.1:c.21-78_21-77del	NP_001265101.1:n.21-78_21-77del
NM_003001.3:c.21-78_21-77del , LRG_317t1:c.21-78_21-77del	NP_002992.1:n.21-78_21-77del
NR_103459.1:n.51-78_51-77del
NM_001035511.2:c.21-78_21-77del	NP_001030588.1:n.21-78_21-77del
NM_001035512.2:c.21-78_21-77del	NP_001030589.1:n.21-78_21-77del
NM_001035513.2:c.20+9111_20+9112del	NP_001030590.1:n.20+9111_20+9112del
NM_001278172.2:c.21-78_21-77del	NP_001265101.1:n.21-78_21-77del
NM_003001.5:c.21-78_21-77del MANE Select	NP_002992.1:n.21-78_21-77del
NR_103459.2:n.46-78_46-77del