Canonical Allele Identifier: CA2813847492

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787905_18787906insTTTTCTTT , CM000681.2:g.18787905_18787906insTTTTCTTT	GRCh38
NC_000019.9:g.18898714_18898715insTTTTCTTT , CM000681.1:g.18898714_18898715insTTTTCTTT	GRCh37
NC_000019.8:g.18759714_18759715insTTTTCTTT	NCBI36
NG_007070.1:g.8407_8408insAAAAGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-249_976-248insAAAAGAAA MANE Select	ENSP00000222271.2:n.976-249_976-248insAAAAGAAA
ENST00000222271.6:c.976-249_976-248insAAAAGAAA	ENSP00000222271.2:n.976-249_976-248insAAAAGAAA
ENST00000425807.1:c.817-249_817-248insAAAAGAAA	ENSP00000403792.1:n.817-249_817-248insAAAAGAAA
ENST00000542601.6:c.877-249_877-248insAAAAGAAA	ENSP00000439156.2:n.877-249_877-248insAAAAGAAA
NM_000095.2:c.976-249_976-248insAAAAGAAA	NP_000086.2:n.976-249_976-248insAAAAGAAA
NM_000095.3:c.976-249_976-248insAAAAGAAA MANE Select	NP_000086.2:n.976-249_976-248insAAAAGAAA