Canonical Allele Identifier: CA404888632
Gene: COMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787605C>A , CM000681.2:g.18787605C>A GRCh38
NC_000019.9:g.18898414C>A , CM000681.1:g.18898414C>A GRCh37
NC_000019.8:g.18759414C>A NCBI36
NG_007070.1:g.8701G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1021G>T MANE Select ENSP00000222271.2:p.Glu341Ter
ENST00000222271.6:c.1021G>T ENSP00000222271.2:p.Glu341Ter
ENST00000425807.1:c.862G>T ENSP00000403792.1:p.Glu288Ter
ENST00000542601.6:c.922G>T ENSP00000439156.2:p.Glu308Ter
NM_000095.2:c.1021G>T NP_000086.2:p.Glu341Ter
NM_000095.3:c.1021G>T MANE Select NP_000086.2:p.Glu341Ter