Canonical Allele Identifier: CA2326526477

Gene: COMP

Linked Data

• dbSNP Id: rs56093208

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787865_18787866insTTCTTTCTTT , CM000681.2:g.18787865_18787866insTTCTTTCTTT	GRCh38
NC_000019.9:g.18898674_18898675insTTCTTTCTTT , CM000681.1:g.18898674_18898675insTTCTTTCTTT	GRCh37
NC_000019.8:g.18759674_18759675insTTCTTTCTTT	NCBI36
NG_007070.1:g.8441_8442insAAGAAAGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-215_976-214insAAGAAAGAAA MANE Select	ENSP00000222271.2:n.976-215_976-214insAAGAAAGAAA
ENST00000222271.6:c.976-215_976-214insAAGAAAGAAA	ENSP00000222271.2:n.976-215_976-214insAAGAAAGAAA
ENST00000425807.1:c.817-215_817-214insAAGAAAGAAA	ENSP00000403792.1:n.817-215_817-214insAAGAAAGAAA
ENST00000542601.6:c.877-215_877-214insAAGAAAGAAA	ENSP00000439156.2:n.877-215_877-214insAAGAAAGAAA
NM_000095.2:c.976-215_976-214insAAGAAAGAAA	NP_000086.2:n.976-215_976-214insAAGAAAGAAA
NM_000095.3:c.976-215_976-214insAAGAAAGAAA MANE Select	NP_000086.2:n.976-215_976-214insAAGAAAGAAA