Canonical Allele Identifier: CA632375808

Gene: COMP

Linked Data

• gnomAD v2: 19-18898701-T-TTTTTTTGAGACAGAGTCTTGCTC
• MyVariant Identifiers: chr19:g.18898701_18898702insTTTTTTGAGACAGAGTCTTGCTC (hg19) ; chr19:g.18787892_18787893insTTTTTTGAGACAGAGTCTTGCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787893_18787894insTTTTTGAGACAGAGTCTTGCTCT , CM000681.2:g.18787893_18787894insTTTTTGAGACAGAGTCTTGCTCT	GRCh38
NC_000019.9:g.18898702_18898703insTTTTTGAGACAGAGTCTTGCTCT , CM000681.1:g.18898702_18898703insTTTTTGAGACAGAGTCTTGCTCT	GRCh37
NC_000019.8:g.18759702_18759703insTTTTTGAGACAGAGTCTTGCTCT	NCBI36
NG_007070.1:g.8413_8414insGAGCAAGACTCTGTCTCAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-243_976-242insGAGCAAGACTCTGTCTCAAAAAA MANE Select	ENSP00000222271.2:n.976-243_976-242insGAGCAAGACTCTGTCTCAAAAAA...
ENST00000222271.6:c.976-243_976-242insGAGCAAGACTCTGTCTCAAAAAA	ENSP00000222271.2:n.976-243_976-242insGAGCAAGACTCTGTCTCAAAAAA...
ENST00000425807.1:c.817-243_817-242insGAGCAAGACTCTGTCTCAAAAAA	ENSP00000403792.1:n.817-243_817-242insGAGCAAGACTCTGTCTCAAAAAA...
ENST00000542601.6:c.877-243_877-242insGAGCAAGACTCTGTCTCAAAAAA	ENSP00000439156.2:n.877-243_877-242insGAGCAAGACTCTGTCTCAAAAAA...
NM_000095.2:c.976-243_976-242insGAGCAAGACTCTGTCTCAAAAAA	NP_000086.2:n.976-243_976-242insGAGCAAGACTCTGTCTCAAAAAA
NM_000095.3:c.976-243_976-242insGAGCAAGACTCTGTCTCAAAAAA MANE Select	NP_000086.2:n.976-243_976-242insGAGCAAGACTCTGTCTCAAAAAA