Canonical Allele Identifier: CA404888648
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787608C>A , CM000681.2:g.18787608C>A GRCh38
NC_000019.9:g.18898417C>A , CM000681.1:g.18898417C>A GRCh37
NC_000019.8:g.18759417C>A NCBI36
NG_007070.1:g.8698G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1018G>T MANE Select ENSP00000222271.2:p.Asp340Tyr
ENST00000222271.6:c.1018G>T ENSP00000222271.2:p.Asp340Tyr
ENST00000425807.1:c.859G>T ENSP00000403792.1:p.Asp287Tyr
ENST00000542601.6:c.919G>T ENSP00000439156.2:p.Asp307Tyr
NM_000095.2:c.1018G>T NP_000086.2:p.Asp340Tyr
NM_000095.3:c.1018G>T MANE Select NP_000086.2:p.Asp340Tyr