Canonical Allele Identifier: CA2326526485

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787867_18787874delinsTTTCTTTC , CM000681.2:g.18787867_18787874delinsTTTCTTTC	GRCh38
NC_000019.9:g.18898676_18898683delinsTTTCTTTC , CM000681.1:g.18898676_18898683delinsTTTCTTTC	GRCh37
NC_000019.8:g.18759676_18759683delinsTTTCTTTC	NCBI36
NG_007070.1:g.8432_8439delinsGAAAGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-224_976-217delinsGAAAGAAA MANE Select	ENSP00000222271.2:n.976-224_976-217delinsGAAAGAAA
ENST00000222271.6:c.976-224_976-217delinsGAAAGAAA	ENSP00000222271.2:n.976-224_976-217delinsGAAAGAAA
ENST00000425807.1:c.817-224_817-217delinsGAAAGAAA	ENSP00000403792.1:n.817-224_817-217delinsGAAAGAAA
ENST00000542601.6:c.877-224_877-217delinsGAAAGAAA	ENSP00000439156.2:n.877-224_877-217delinsGAAAGAAA
NM_000095.2:c.976-224_976-217delinsGAAAGAAA	NP_000086.2:n.976-224_976-217delinsGAAAGAAA
NM_000095.3:c.976-224_976-217delinsGAAAGAAA MANE Select	NP_000086.2:n.976-224_976-217delinsGAAAGAAA