Canonical Allele Identifier: CA306256967

Gene: COMP

Linked Data

• dbSNP Id: rs56093208
• gnomAD v3: 19-18787864-C-CTTTT
• gnomAD v4: 19-18787864-C-CTTTT
• MyVariant Identifiers: chr19:g.18898674_18898675insTTTT (hg19) ; chr19:g.18898673_18898674insTTTT (hg19) ; chr19:g.18787865_18787866insTTTT (hg38) ; chr19:g.18787864_18787865insTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787865_18787866insTTTT , CM000681.2:g.18787865_18787866insTTTT	GRCh38
NC_000019.9:g.18898674_18898675insTTTT , CM000681.1:g.18898674_18898675insTTTT	GRCh37
NC_000019.8:g.18759674_18759675insTTTT	NCBI36
NG_007070.1:g.8441_8442insAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-215_976-214insAAAA MANE Select	ENSP00000222271.2:n.976-215_976-214insAAAA
ENST00000222271.6:c.976-215_976-214insAAAA	ENSP00000222271.2:n.976-215_976-214insAAAA
ENST00000425807.1:c.817-215_817-214insAAAA	ENSP00000403792.1:n.817-215_817-214insAAAA
ENST00000542601.6:c.877-215_877-214insAAAA	ENSP00000439156.2:n.877-215_877-214insAAAA
NM_000095.2:c.976-215_976-214insAAAA	NP_000086.2:n.976-215_976-214insAAAA
NM_000095.3:c.976-215_976-214insAAAA MANE Select	NP_000086.2:n.976-215_976-214insAAAA