Canonical Allele Identifier: CA2326526513

Gene: COMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787874_18787876delinsCTT , CM000681.2:g.18787874_18787876delinsCTT	GRCh38
NC_000019.9:g.18898683_18898685delinsCTT , CM000681.1:g.18898683_18898685delinsCTT	GRCh37
NC_000019.8:g.18759683_18759685delinsCTT	NCBI36
NG_007070.1:g.8430_8432delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.976-226_976-224delinsAAG MANE Select	ENSP00000222271.2:n.976-226_976-224delinsAAG
ENST00000222271.6:c.976-226_976-224delinsAAG	ENSP00000222271.2:n.976-226_976-224delinsAAG
ENST00000425807.1:c.817-226_817-224delinsAAG	ENSP00000403792.1:n.817-226_817-224delinsAAG
ENST00000542601.6:c.877-226_877-224delinsAAG	ENSP00000439156.2:n.877-226_877-224delinsAAG
NM_000095.2:c.976-226_976-224delinsAAG	NP_000086.2:n.976-226_976-224delinsAAG
NM_000095.3:c.976-226_976-224delinsAAG MANE Select	NP_000086.2:n.976-226_976-224delinsAAG