Canonical Allele Identifier: CA404888653
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787610G>T , CM000681.2:g.18787610G>T GRCh38
NC_000019.9:g.18898419G>T , CM000681.1:g.18898419G>T GRCh37
NC_000019.8:g.18759419G>T NCBI36
NG_007070.1:g.8696C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1016C>A MANE Select ENSP00000222271.2:p.Thr339Lys
ENST00000222271.6:c.1016C>A ENSP00000222271.2:p.Thr339Lys
ENST00000425807.1:c.857C>A ENSP00000403792.1:p.Thr286Lys
ENST00000542601.6:c.917C>A ENSP00000439156.2:p.Thr306Lys
NM_000095.2:c.1016C>A NP_000086.2:p.Thr339Lys
NM_000095.3:c.1016C>A MANE Select NP_000086.2:p.Thr339Lys