Canonical Allele Identifier: CA404888658
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787611T>C , CM000681.2:g.18787611T>C GRCh38
NC_000019.9:g.18898420T>C , CM000681.1:g.18898420T>C GRCh37
NC_000019.8:g.18759420T>C NCBI36
NG_007070.1:g.8695A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1015A>G MANE Select ENSP00000222271.2:p.Thr339Ala
ENST00000222271.6:c.1015A>G ENSP00000222271.2:p.Thr339Ala
ENST00000425807.1:c.856A>G ENSP00000403792.1:p.Thr286Ala
ENST00000542601.6:c.916A>G ENSP00000439156.2:p.Thr306Ala
NM_000095.2:c.1015A>G NP_000086.2:p.Thr339Ala
NM_000095.3:c.1015A>G MANE Select NP_000086.2:p.Thr339Ala