Canonical Allele Identifier: CA404888221
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787562T>A , CM000681.2:g.18787562T>A GRCh38
NC_000019.9:g.18898371T>A , CM000681.1:g.18898371T>A GRCh37
NC_000019.8:g.18759371T>A NCBI36
NG_007070.1:g.8744A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1064A>T MANE Select ENSP00000222271.2:p.Lys355Met
ENST00000222271.6:c.1064A>T ENSP00000222271.2:p.Lys355Met
ENST00000425807.1:c.905A>T ENSP00000403792.1:p.Lys302Met
ENST00000542601.6:c.965A>T ENSP00000439156.2:p.Lys322Met
NM_000095.2:c.1064A>T NP_000086.2:p.Lys355Met
NM_000095.3:c.1064A>T MANE Select NP_000086.2:p.Lys355Met