Canonical Allele Identifier: CA2326525603
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786165A= , CM000681.2:g.18786165A= GRCh38
NC_000019.9:g.18896975A= , CM000681.1:g.18896975A= GRCh37
NC_000019.8:g.18757975A= NCBI36
NG_007070.1:g.10140T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1308-19T= MANE Select ENSP00000222271.2:n.1308-19T=
ENST00000222271.6:c.1308-19T= ENSP00000222271.2:n.1308-19T=
ENST00000425807.1:c.1149-19T= ENSP00000403792.1:n.1149-19T=
ENST00000542601.6:c.1209-19T= ENSP00000439156.2:n.1209-19T=
ENST00000612179.1:n.558-19T=
NM_000095.2:c.1308-19T= NP_000086.2:n.1308-19T=
NM_000095.3:c.1308-19T= MANE Select NP_000086.2:n.1308-19T=