Canonical Allele Identifier: CA920074426
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1568555803
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787874del , CM000681.2:g.18787874del GRCh38
NC_000019.9:g.18898683del , CM000681.1:g.18898683del GRCh37
NC_000019.8:g.18759683del NCBI36
NG_007070.1:g.8432del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-224del MANE Select ENSP00000222271.2:n.976-224del
ENST00000222271.6:c.976-224del ENSP00000222271.2:n.976-224del
ENST00000425807.1:c.817-224del ENSP00000403792.1:n.817-224del
ENST00000542601.6:c.877-224del ENSP00000439156.2:n.877-224del
NM_000095.2:c.976-224del NP_000086.2:n.976-224del
NM_000095.3:c.976-224del MANE Select NP_000086.2:n.976-224del
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