Canonical Allele Identifier: CA404896540
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18789258T>C , CM000681.2:g.18789258T>C GRCh38
NC_000019.9:g.18900067T>C , CM000681.1:g.18900067T>C GRCh37
NC_000019.8:g.18761067T>C NCBI36
NG_007070.1:g.7048A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.430A>G MANE Select ENSP00000222271.2:p.Asn144Asp
ENST00000222271.6:c.430A>G ENSP00000222271.2:p.Asn144Asp
ENST00000425807.1:c.391-366A>G ENSP00000403792.1:n.391-366A>G
ENST00000542601.6:c.331A>G ENSP00000439156.2:p.Asn111Asp
NM_000095.2:c.430A>G NP_000086.2:p.Asn144Asp
NM_000095.3:c.430A>G MANE Select NP_000086.2:p.Asn144Asp