Canonical Allele Identifier: CA2326525593
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786156_18786160delinsATAGG , CM000681.2:g.18786156_18786160delinsATAGG GRCh38
NC_000019.9:g.18896966_18896970delinsATAGG , CM000681.1:g.18896966_18896970delinsATAGG GRCh37
NC_000019.8:g.18757966_18757970delinsATAGG NCBI36
NG_007070.1:g.10145_10149delinsCCTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1308-14_1308-10delinsCCTAT MANE Select ENSP00000222271.2:n.1308-14_1308-10delinsCCTAT
ENST00000222271.6:c.1308-14_1308-10delinsCCTAT ENSP00000222271.2:n.1308-14_1308-10delinsCCTAT
ENST00000425807.1:c.1149-14_1149-10delinsCCTAT ENSP00000403792.1:n.1149-14_1149-10delinsCCTAT
ENST00000542601.6:c.1209-14_1209-10delinsCCTAT ENSP00000439156.2:n.1209-14_1209-10delinsCCTAT
ENST00000612179.1:n.558-14_558-10delinsCCTAT
NM_000095.2:c.1308-14_1308-10delinsCCTAT NP_000086.2:n.1308-14_1308-10delinsCCTAT
NM_000095.3:c.1308-14_1308-10delinsCCTAT MANE Select NP_000086.2:n.1308-14_1308-10delinsCCTAT
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