Canonical Allele Identifier: CA2326525607

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786168_18786170delinsCAG , CM000681.2:g.18786168_18786170delinsCAG	GRCh38
NC_000019.9:g.18896978_18896980delinsCAG , CM000681.1:g.18896978_18896980delinsCAG	GRCh37
NC_000019.8:g.18757978_18757980delinsCAG	NCBI36
NG_007070.1:g.10135_10137delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000222271.7:c.1308-24_1308-22delinsCTG MANE Select	ENSP00000222271.2:n.1308-24_1308-22delinsCTG
ENST00000222271.6:c.1308-24_1308-22delinsCTG	ENSP00000222271.2:n.1308-24_1308-22delinsCTG
ENST00000425807.1:c.1149-24_1149-22delinsCTG	ENSP00000403792.1:n.1149-24_1149-22delinsCTG
ENST00000542601.6:c.1209-24_1209-22delinsCTG	ENSP00000439156.2:n.1209-24_1209-22delinsCTG
ENST00000612179.1:n.558-24_558-22delinsCTG
NM_000095.2:c.1308-24_1308-22delinsCTG	NP_000086.2:n.1308-24_1308-22delinsCTG
NM_000095.3:c.1308-24_1308-22delinsCTG MANE Select	NP_000086.2:n.1308-24_1308-22delinsCTG