Canonical Allele Identifier: CA732364763

Gene: COQ8A

Linked Data

• dbSNP Id: rs1296943147
• MyVariant Identifiers: chr1:g.227170820_227170821insCA (hg19) ; chr1:g.226983119_226983120insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226983121_226983122dup , CM000663.2:g.226983121_226983122dup	GRCh38
NC_000001.10:g.227170822_227170823dup , CM000663.1:g.227170822_227170823dup	GRCh37
NC_000001.9:g.225237445_225237446dup	NCBI36
NG_012825.1:g.47885_47886dup
NG_012825.2:g.90586_90587dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366777.4:c.1080+87_1080+88dup MANE Select	ENSP00000355739.3:n.1080+87_1080+88dup
ENST00000366779.6:c.*5807+87_*5807+88dup	ENSP00000355741.2:n.*5807+87_*5807+88dup
ENST00000676884.1:c.*5929+87_*5929+88dup	ENSP00000503200.1:n.*5929+87_*5929+88dup
ENST00000366777.3:c.1080+87_1080+88dup	ENSP00000355739.3:n.1080+87_1080+88dup
ENST00000366778.5:c.924+87_924+88dup	ENSP00000355740.1:n.924+87_924+88dup
ENST00000366779.5:c.1080+87_1080+88dup	ENSP00000355741.1:n.1080+87_1080+88dup
ENST00000478406.5:n.1146_1147dup
ENST00000479852.1:n.28+87_28+88dup
ENST00000485462.5:n.470+87_470+88dup
NM_020247.4:c.1080+87_1080+88dup	NP_064632.2:n.1080+87_1080+88dup
XM_005273201.1:c.1080+87_1080+88dup	XP_005273258.1:n.1080+87_1080+88dup
XM_011544238.1:c.1080+87_1080+88dup	XP_011542540.1:n.1080+87_1080+88dup
XM_011544239.1:c.1080+87_1080+88dup	XP_011542541.1:n.1080+87_1080+88dup
XM_011544240.1:c.1080+87_1080+88dup	XP_011542542.1:n.1080+87_1080+88dup
XM_011544241.1:c.1080+87_1080+88dup	XP_011542543.1:n.1080+87_1080+88dup
XM_011544239.2:c.1080+87_1080+88dup	XP_011542541.1:n.1080+87_1080+88dup
XM_011544241.2:c.1080+87_1080+88dup	XP_011542543.1:n.1080+87_1080+88dup
XM_017001852.1:c.1080+87_1080+88dup	XP_016857341.1:n.1080+87_1080+88dup
XM_024448517.1:c.1080+87_1080+88dup	XP_024304285.1:n.1080+87_1080+88dup
XM_024448518.1:c.1080+87_1080+88dup	XP_024304286.1:n.1080+87_1080+88dup
NM_020247.5:c.1080+87_1080+88dup MANE Select	NP_064632.2:n.1080+87_1080+88dup