Canonical Allele Identifier: CA994238076

Gene: COMP

Linked Data

• gnomAD v3: 19-18787916-T-TTCTTTCTTTC
• gnomAD v4: 19-18787916-T-TTCTTTCTTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787917_18787918insCTTTCTTTCT , CM000681.2:g.18787917_18787918insCTTTCTTTCT	GRCh38
NC_000019.9:g.18898726_18898727insCTTTCTTTCT , CM000681.1:g.18898726_18898727insCTTTCTTTCT	GRCh37
NC_000019.8:g.18759726_18759727insCTTTCTTTCT	NCBI36
NG_007070.1:g.8389_8390insGAAAGAAAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-267_976-266insGAAAGAAAGA MANE Select	ENSP00000222271.2:n.976-267_976-266insGAAAGAAAGA
ENST00000222271.6:c.976-267_976-266insGAAAGAAAGA	ENSP00000222271.2:n.976-267_976-266insGAAAGAAAGA
ENST00000425807.1:c.817-267_817-266insGAAAGAAAGA	ENSP00000403792.1:n.817-267_817-266insGAAAGAAAGA
ENST00000542601.6:c.877-267_877-266insGAAAGAAAGA	ENSP00000439156.2:n.877-267_877-266insGAAAGAAAGA
NM_000095.2:c.976-267_976-266insGAAAGAAAGA	NP_000086.2:n.976-267_976-266insGAAAGAAAGA
NM_000095.3:c.976-267_976-266insGAAAGAAAGA MANE Select	NP_000086.2:n.976-267_976-266insGAAAGAAAGA