Canonical Allele Identifier: CA2813847490

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787893_18787894insTTTT , CM000681.2:g.18787893_18787894insTTTT	GRCh38
NC_000019.9:g.18898702_18898703insTTTT , CM000681.1:g.18898702_18898703insTTTT	GRCh37
NC_000019.8:g.18759702_18759703insTTTT	NCBI36
NG_007070.1:g.8415_8416insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-241_976-240insAAAA MANE Select	ENSP00000222271.2:n.976-241_976-240insAAAA
ENST00000222271.6:c.976-241_976-240insAAAA	ENSP00000222271.2:n.976-241_976-240insAAAA
ENST00000425807.1:c.817-241_817-240insAAAA	ENSP00000403792.1:n.817-241_817-240insAAAA
ENST00000542601.6:c.877-241_877-240insAAAA	ENSP00000439156.2:n.877-241_877-240insAAAA
NM_000095.2:c.976-241_976-240insAAAA	NP_000086.2:n.976-241_976-240insAAAA
NM_000095.3:c.976-241_976-240insAAAA MANE Select	NP_000086.2:n.976-241_976-240insAAAA