Canonical Allele Identifier: CA2326526398

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787459_18787460delinsTC , CM000681.2:g.18787459_18787460delinsTC	GRCh38
NC_000019.9:g.18898268_18898269delinsTC , CM000681.1:g.18898268_18898269delinsTC	GRCh37
NC_000019.8:g.18759268_18759269delinsTC	NCBI36
NG_007070.1:g.8846_8847delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1135+31_1135+32delinsGA MANE Select	ENSP00000222271.2:n.1135+31_1135+32delinsGA
ENST00000222271.6:c.1135+31_1135+32delinsGA	ENSP00000222271.2:n.1135+31_1135+32delinsGA
ENST00000425807.1:c.976+31_976+32delinsGA	ENSP00000403792.1:n.976+31_976+32delinsGA
ENST00000542601.6:c.1036+31_1036+32delinsGA	ENSP00000439156.2:n.1036+31_1036+32delinsGA
NM_000095.2:c.1135+31_1135+32delinsGA	NP_000086.2:n.1135+31_1135+32delinsGA
NM_000095.3:c.1135+31_1135+32delinsGA MANE Select	NP_000086.2:n.1135+31_1135+32delinsGA