Canonical Allele Identifier: CA14936128

Gene: CHCHD10

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23767275T>C , CM000684.2:g.23767275T>C	GRCh38
NC_000022.10:g.24109462T>C , CM000684.1:g.24109462T>C	GRCh37
NC_000022.9:g.22439462T>C	NCBI36
NG_034223.1:g.5698A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000484558.3:c.261+99A>G MANE Select	ENSP00000418428.3:n.261+99A>G
ENST00000401675.7:c.261+99A>G	ENSP00000384973.3:n.261+99A>G
ENST00000484558.2:c.261+99A>G	ENSP00000418428.2:n.261+99A>G
ENST00000517886.1:c.208+99A>G	ENSP00000429976.1:n.208+99A>G
ENST00000520222.1:c.41+559A>G	ENSP00000430042.1:n.41+559A>G
NM_001301339.1:c.261+99A>G	NP_001288268.1:n.261+99A>G
NM_213720.2:c.261+99A>G	NP_998885.1:n.261+99A>G
NR_125755.1:n.306+99A>G
NR_125756.1:n.139+559A>G
NM_001301339.2:c.261+99A>G	NP_001288268.1:n.261+99A>G
NM_213720.3:c.261+99A>G MANE Select	NP_998885.1:n.261+99A>G
NR_125755.2:n.306+99A>G
NR_125756.2:n.139+559A>G