Canonical Allele Identifier: CA410916220

Gene: CHCHD10

Linked Data

• MyVariant Identifiers: chr22:g.24109629T>G (hg19) ; chr22:g.23767442T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23767442T>G , CM000684.2:g.23767442T>G	GRCh38
NC_000022.10:g.24109629T>G , CM000684.1:g.24109629T>G	GRCh37
NC_000022.9:g.22439629T>G	NCBI36
NG_034223.1:g.5531A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000484558.3:c.193A>C MANE Select	ENSP00000418428.3:p.Met65Leu
ENST00000401675.7:c.193A>C	ENSP00000384973.3:p.Met65Leu
ENST00000484558.2:c.193A>C	ENSP00000418428.2:p.Met65Leu
ENST00000517886.1:c.140A>C	ENSP00000429976.1:p.His47Pro
ENST00000520222.1:c.41+392A>C	ENSP00000430042.1:n.41+392A>C
NM_001301339.1:c.193A>C	NP_001288268.1:p.Met65Leu
NM_213720.2:c.193A>C	NP_998885.1:p.Met65Leu
NR_125755.1:n.238A>C
NR_125756.1:n.139+392A>C
NM_001301339.2:c.193A>C	NP_001288268.1:p.Met65Leu
NM_213720.3:c.193A>C MANE Select	NP_998885.1:p.Met65Leu
NR_125755.2:n.238A>C
NR_125756.2:n.139+392A>C