Canonical Allele Identifier: CA1225123763

Gene: COQ8A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226983473_226983474delinsTG , CM000663.2:g.226983473_226983474delinsTG	GRCh38
NC_000001.10:g.227171174_227171175delinsTG , CM000663.1:g.227171174_227171175delinsTG	GRCh37
NC_000001.9:g.225237797_225237798delinsTG	NCBI36
NG_012825.1:g.48237_48238delinsTG
NG_012825.2:g.90938_90939delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000366777.4:c.1081-79_1081-78delinsTG MANE Select	ENSP00000355739.3:n.1081-79_1081-78delins...
ENST00000366779.6:c.*5808-79_*5808-78delinsTG	ENSP00000355741.2:n.*5808-79_*5808-78deli...
ENST00000676884.1:c.*5930-79_*5930-78delinsTG	ENSP00000503200.1:n.*5930-79_*5930-78deli...
ENST00000366777.3:c.1081-79_1081-78delinsTG	ENSP00000355739.3:n.1081-79_1081-78delins...
ENST00000366778.5:c.925-79_925-78delinsTG	ENSP00000355740.1:n.925-79_925-78delinsTG...
ENST00000366779.5:c.1081-79_1081-78delinsTG	ENSP00000355741.1:n.1081-79_1081-78delins...
ENST00000478406.5:n.1498_1499delinsTG
ENST00000479852.1:n.29-79_29-78delinsTG
ENST00000485462.5:n.471-79_471-78delinsTG
NM_020247.4:c.1081-79_1081-78delinsTG	NP_064632.2:n.1081-79_1081-78delinsTG
XM_005273201.1:c.1081-79_1081-78delinsTG	XP_005273258.1:n.1081-79_1081-78delinsTG
XM_011544238.1:c.1081-79_1081-78delinsTG	XP_011542540.1:n.1081-79_1081-78delinsTG
XM_011544239.1:c.1081-79_1081-78delinsTG	XP_011542541.1:n.1081-79_1081-78delinsTG
XM_011544240.1:c.1081-79_1081-78delinsTG	XP_011542542.1:n.1081-79_1081-78delinsTG
XM_011544241.1:c.1081-79_1081-78delinsTG	XP_011542543.1:n.1081-79_1081-78delinsTG
XM_011544239.2:c.1081-79_1081-78delinsTG	XP_011542541.1:n.1081-79_1081-78delinsTG
XM_011544241.2:c.1081-79_1081-78delinsTG	XP_011542543.1:n.1081-79_1081-78delinsTG
XM_017001852.1:c.1081-79_1081-78delinsTG	XP_016857341.1:n.1081-79_1081-78delinsTG
XM_024448517.1:c.1081-79_1081-78delinsTG	XP_024304285.1:n.1081-79_1081-78delinsTG
XM_024448518.1:c.1081-79_1081-78delinsTG	XP_024304286.1:n.1081-79_1081-78delinsTG
NM_020247.5:c.1081-79_1081-78delinsTG MANE Select	NP_064632.2:n.1081-79_1081-78delinsTG