Canonical Allele Identifier: CA2326526569

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787907_18787914delinsTTTCTTTC , CM000681.2:g.18787907_18787914delinsTTTCTTTC	GRCh38
NC_000019.9:g.18898716_18898723delinsTTTCTTTC , CM000681.1:g.18898716_18898723delinsTTTCTTTC	GRCh37
NC_000019.8:g.18759716_18759723delinsTTTCTTTC	NCBI36
NG_007070.1:g.8392_8399delinsGAAAGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-264_976-257delinsGAAAGAAA MANE Select	ENSP00000222271.2:n.976-264_976-257delinsGAAAGAAA
ENST00000222271.6:c.976-264_976-257delinsGAAAGAAA	ENSP00000222271.2:n.976-264_976-257delinsGAAAGAAA
ENST00000425807.1:c.817-264_817-257delinsGAAAGAAA	ENSP00000403792.1:n.817-264_817-257delinsGAAAGAAA
ENST00000542601.6:c.877-264_877-257delinsGAAAGAAA	ENSP00000439156.2:n.877-264_877-257delinsGAAAGAAA
NM_000095.2:c.976-264_976-257delinsGAAAGAAA	NP_000086.2:n.976-264_976-257delinsGAAAGAAA
NM_000095.3:c.976-264_976-257delinsGAAAGAAA MANE Select	NP_000086.2:n.976-264_976-257delinsGAAAGAAA