Canonical Allele Identifier: CA2580099258

Gene: CHCHD10

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23767363_23767364delinsCT , CM000684.2:g.23767363_23767364delinsCT	GRCh38
NC_000022.10:g.24109550_24109551delinsCT , CM000684.1:g.24109550_24109551delinsCT	GRCh37
NC_000022.9:g.22439550_22439551delinsCT	NCBI36
NG_034223.1:g.5609_5610delinsAG

Transcript Alleles

HGVS	Amino-acid Change
NM_213720.3:c.261+10_261+11delinsAG MANE Select	NP_998885.1:n.261+10_261+11delinsAG
ENST00000484558.3:c.261+10_261+11delinsAG MANE Select	ENSP00000418428.3:n.261+10_261+11delinsAG
NM_001301339.1:c.261+10_261+11delinsAG	NP_001288268.1:n.261+10_261+11delinsAG
NM_001301339.2:c.261+10_261+11delinsAG	NP_001288268.1:n.261+10_261+11delinsAG
NM_213720.2:c.261+10_261+11delinsAG	NP_998885.1:n.261+10_261+11delinsAG
NR_125755.1:n.306+10_306+11delinsAG
NR_125755.2:n.306+10_306+11delinsAG
NR_125756.1:n.139+470_139+471delinsAG
NR_125756.2:n.139+470_139+471delinsAG
ENST00000401675.7:c.261+10_261+11delinsAG	ENSP00000384973.3:n.261+10_261+11delinsAG
ENST00000484558.2:c.261+10_261+11delinsAG	ENSP00000418428.2:n.261+10_261+11delinsAG
ENST00000517886.1:c.208+10_208+11delinsAG	ENSP00000429976.1:n.208+10_208+11delinsAG
ENST00000520222.1:c.41+470_41+471delinsAG	ENSP00000430042.1:n.41+470_41+471delinsAG