Canonical Allele Identifier: CA2326525611
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18786178G= , CM000681.2:g.18786178G= GRCh38
NC_000019.9:g.18896988G= , CM000681.1:g.18896988G= GRCh37
NC_000019.8:g.18757988G= NCBI36
NG_007070.1:g.10127C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1308-32C= MANE Select ENSP00000222271.2:n.1308-32C=
ENST00000222271.6:c.1308-32C= ENSP00000222271.2:n.1308-32C=
ENST00000425807.1:c.1149-32C= ENSP00000403792.1:n.1149-32C=
ENST00000542601.6:c.1209-32C= ENSP00000439156.2:n.1209-32C=
ENST00000612179.1:n.558-32C=
NM_000095.2:c.1308-32C= NP_000086.2:n.1308-32C=
NM_000095.3:c.1308-32C= MANE Select NP_000086.2:n.1308-32C=