Canonical Allele Identifier: CA1012968121
Gene: COQ8A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226983431_226983473dup , CM000663.2:g.226983431_226983473dup GRCh38
NC_000001.10:g.227171132_227171174dup , CM000663.1:g.227171132_227171174dup GRCh37
NC_000001.9:g.225237755_225237797dup NCBI36
NG_012825.1:g.48195_48237dup
NG_012825.2:g.90896_90938dup

Transcript Alleles

HGVS Amino-acid change
ENST00000366777.4:c.1081-121_1081-79dup MANE Select ENSP00000355739.3:n.1081-121_1081-79dup
ENST00000366779.6:c.*5808-121_*5808-79dup ENSP00000355741.2:n.*5808-121_*5808-79dup...
ENST00000676884.1:c.*5930-121_*5930-79dup ENSP00000503200.1:n.*5930-121_*5930-79dup...
ENST00000366777.3:c.1081-121_1081-79dup ENSP00000355739.3:n.1081-121_1081-79dup
ENST00000366778.5:c.925-121_925-79dup ENSP00000355740.1:n.925-121_925-79dup
ENST00000366779.5:c.1081-121_1081-79dup ENSP00000355741.1:n.1081-121_1081-79dup
ENST00000478406.5:n.1456_1498dup
ENST00000479852.1:n.29-121_29-79dup
ENST00000485462.5:n.471-121_471-79dup
NM_020247.4:c.1081-121_1081-79dup NP_064632.2:n.1081-121_1081-79dup
XM_005273201.1:c.1081-121_1081-79dup XP_005273258.1:n.1081-121_1081-79dup
XM_011544238.1:c.1081-121_1081-79dup XP_011542540.1:n.1081-121_1081-79dup
XM_011544239.1:c.1081-121_1081-79dup XP_011542541.1:n.1081-121_1081-79dup
XM_011544240.1:c.1081-121_1081-79dup XP_011542542.1:n.1081-121_1081-79dup
XM_011544241.1:c.1081-121_1081-79dup XP_011542543.1:n.1081-121_1081-79dup
XM_011544239.2:c.1081-121_1081-79dup XP_011542541.1:n.1081-121_1081-79dup
XM_011544241.2:c.1081-121_1081-79dup XP_011542543.1:n.1081-121_1081-79dup
XM_017001852.1:c.1081-121_1081-79dup XP_016857341.1:n.1081-121_1081-79dup
XM_024448517.1:c.1081-121_1081-79dup XP_024304285.1:n.1081-121_1081-79dup
XM_024448518.1:c.1081-121_1081-79dup XP_024304286.1:n.1081-121_1081-79dup
NM_020247.5:c.1081-121_1081-79dup MANE Select NP_064632.2:n.1081-121_1081-79dup