Canonical Allele Identifier: CA1202692523

Gene: SDHC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161323639_161323640delinsGC , CM000663.2:g.161323639_161323640delinsGC	GRCh38
NC_000001.10:g.161293429_161293430delinsGC , CM000663.1:g.161293429_161293430delinsGC	GRCh37
NC_000001.9:g.159560053_159560054delinsGC	NCBI36
NG_012767.1:g.14264_14265delinsGC , LRG_317:g.14264_14265delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470743.5:c.46_47delinsGC	ENSP00000482902.2:p.Ala16=
ENST00000367975.7:c.46_47delinsGC MANE Select	ENSP00000356953.3:p.Ala16=
ENST00000342751.8:c.46_47delinsGC	ENSP00000356952.3:p.Ala16=
ENST00000367975.6:c.46_47delinsGC	ENSP00000356953.2:p.Ala16=
ENST00000392169.6:c.20+9214_20+9215delinsGC	ENSP00000376009.2:n.20+9214_20+9215delinsGC
ENST00000432287.6:c.46_47delinsGC	ENSP00000390558.2:p.Ala16=
ENST00000470743.4:c.26_27delinsGC
ENST00000504963.5:c.46_47delinsGC	ENSP00000423929.1:p.Ala16=
ENST00000513009.5:c.46_47delinsGC	ENSP00000423260.1:p.Ala16=
ENST00000515731.1:n.520_521delinsGC
NM_001035511.1:c.46_47delinsGC	NP_001030588.1:p.Ala16=
NM_001035512.1:c.46_47delinsGC	NP_001030589.1:p.Ala16=
NM_001035513.1:c.20+9214_20+9215delinsGC	NP_001030590.1:n.20+9214_20+9215delinsGC
NM_001278172.1:c.46_47delinsGC	NP_001265101.1:p.Ala16=
NM_003001.3:c.46_47delinsGC , LRG_317t1:c.46_47delinsGC	NP_002992.1:p.Ala16=
NR_103459.1:n.76_77delinsGC
NM_001035511.2:c.46_47delinsGC	NP_001030588.1:p.Ala16=
NM_001035512.2:c.46_47delinsGC	NP_001030589.1:p.Ala16=
NM_001035513.2:c.20+9214_20+9215delinsGC	NP_001030590.1:n.20+9214_20+9215delinsGC
NM_001278172.2:c.46_47delinsGC	NP_001265101.1:p.Ala16=
NM_003001.5:c.46_47delinsGC MANE Select	NP_002992.1:p.Ala16=
NR_103459.2:n.71_72delinsGC