Canonical Allele Identifier: CA2326526106
Gene: COMP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787604T= , CM000681.2:g.18787604T= GRCh38
NC_000019.9:g.18898413T= , CM000681.1:g.18898413T= GRCh37
NC_000019.8:g.18759413T= NCBI36
NG_007070.1:g.8702A=

Transcript Alleles

HGVS Amino-acid change
ENST00000222271.7:c.1022A= MANE Select ENSP00000222271.2:p.Glu341=
ENST00000222271.6:c.1022A= ENSP00000222271.2:p.Glu341=
ENST00000425807.1:c.863A= ENSP00000403792.1:p.Glu288=
ENST00000542601.6:c.923A= ENSP00000439156.2:p.Glu308=
NM_000095.2:c.1022A= NP_000086.2:p.Glu341=
NM_000095.3:c.1022A= MANE Select NP_000086.2:p.Glu341=