Canonical Allele Identifier: CA2326526441
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787860_18787890delinsTTTTCTCTTTCTTTCTTTCTTTCTTTCTTTC , CM000681.2:g.18787860_18787890delinsTTTTCTCTTTCTTTCTTTCTTTCTTTCTTTC GRCh38
NC_000019.9:g.18898669_18898699delinsTTTTCTCTTTCTTTCTTTCTTTCTTTCTTTC , CM000681.1:g.18898669_18898699delinsTTTTCTCTTTCTTTCTTTCTTTCTTTCTTTC GRCh37
NC_000019.8:g.18759669_18759699delinsTTTTCTCTTTCTTTCTTTCTTTCTTTCTTTC NCBI36
NG_007070.1:g.8416_8446delinsGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-240_976-210delinsGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAA MANE Select ENSP00000222271.2:n.976-240_976-210delinsGAAAGAAAGAAAGAAAGAAA...
ENST00000222271.6:c.976-240_976-210delinsGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAA ENSP00000222271.2:n.976-240_976-210delinsGAAAGAAAGAAAGAAAGAAA...
ENST00000425807.1:c.817-240_817-210delinsGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAA ENSP00000403792.1:n.817-240_817-210delinsGAAAGAAAGAAAGAAAGAAA...
ENST00000542601.6:c.877-240_877-210delinsGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAA ENSP00000439156.2:n.877-240_877-210delinsGAAAGAAAGAAAGAAAGAAA...
NM_000095.2:c.976-240_976-210delinsGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAA NP_000086.2:n.976-240_976-210delinsGAAAGAAAGAAAGAAAGAAAGAAAGA...
NM_000095.3:c.976-240_976-210delinsGAAAGAAAGAAAGAAAGAAAGAAAGAGAAAA MANE Select NP_000086.2:n.976-240_976-210delinsGAAAGAAAGAAAGAAAGAAAGAAAGA...