Canonical Allele Identifier: CA2326526491
Gene: COMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787870_18787872delinsCTT , CM000681.2:g.18787870_18787872delinsCTT GRCh38
NC_000019.9:g.18898679_18898681delinsCTT , CM000681.1:g.18898679_18898681delinsCTT GRCh37
NC_000019.8:g.18759679_18759681delinsCTT NCBI36
NG_007070.1:g.8434_8436delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-222_976-220delinsAAG MANE Select ENSP00000222271.2:n.976-222_976-220delinsAAG
ENST00000222271.6:c.976-222_976-220delinsAAG ENSP00000222271.2:n.976-222_976-220delinsAAG
ENST00000425807.1:c.817-222_817-220delinsAAG ENSP00000403792.1:n.817-222_817-220delinsAAG
ENST00000542601.6:c.877-222_877-220delinsAAG ENSP00000439156.2:n.877-222_877-220delinsAAG
NM_000095.2:c.976-222_976-220delinsAAG NP_000086.2:n.976-222_976-220delinsAAG
NM_000095.3:c.976-222_976-220delinsAAG MANE Select NP_000086.2:n.976-222_976-220delinsAAG
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