Canonical Allele Identifier: CA2741617860

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787824C>A , CM000681.2:g.18787824C>A	GRCh38
NC_000019.9:g.18898633C>A , CM000681.1:g.18898633C>A	GRCh37
NC_000019.8:g.18759633C>A	NCBI36
NG_007070.1:g.8482G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-174G>T MANE Select	ENSP00000222271.2:n.976-174G>T
ENST00000222271.6:c.976-174G>T	ENSP00000222271.2:n.976-174G>T
ENST00000425807.1:c.817-174G>T	ENSP00000403792.1:n.817-174G>T
ENST00000542601.6:c.877-174G>T	ENSP00000439156.2:n.877-174G>T
NM_000095.2:c.976-174G>T	NP_000086.2:n.976-174G>T
NM_000095.3:c.976-174G>T MANE Select	NP_000086.2:n.976-174G>T