Canonical Allele Identifier: CA404887984
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787531G>C , CM000681.2:g.18787531G>C GRCh38
NC_000019.9:g.18898340G>C , CM000681.1:g.18898340G>C GRCh37
NC_000019.8:g.18759340G>C NCBI36
NG_007070.1:g.8775C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1095C>G MANE Select ENSP00000222271.2:p.Asp365Glu
ENST00000222271.6:c.1095C>G ENSP00000222271.2:p.Asp365Glu
ENST00000425807.1:c.936C>G ENSP00000403792.1:p.Asp312Glu
ENST00000542601.6:c.996C>G ENSP00000439156.2:p.Asp332Glu
NM_000095.2:c.1095C>G NP_000086.2:p.Asp365Glu
NM_000095.3:c.1095C>G MANE Select NP_000086.2:p.Asp365Glu