Canonical Allele Identifier: CA2583621932

Gene: COMP

Linked Data

• gnomAD v4: 19-18786206-TACCCGGACGCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18786211_18786222del , CM000681.2:g.18786211_18786222del	GRCh38
NC_000019.9:g.18897021_18897032del , CM000681.1:g.18897021_18897032del	GRCh37
NC_000019.8:g.18758021_18758032del	NCBI36
NG_007070.1:g.10087_10098del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1307+21_1307+32del MANE Select	ENSP00000222271.2:n.1307+21_1307+32del
ENST00000222271.6:c.1307+21_1307+32del	ENSP00000222271.2:n.1307+21_1307+32del
ENST00000425807.1:c.1148+21_1148+32del	ENSP00000403792.1:n.1148+21_1148+32del
ENST00000542601.6:c.1208+21_1208+32del	ENSP00000439156.2:n.1208+21_1208+32del
ENST00000612179.1:n.557+21_557+32del
NM_000095.2:c.1307+21_1307+32del	NP_000086.2:n.1307+21_1307+32del
NM_000095.3:c.1307+21_1307+32del MANE Select	NP_000086.2:n.1307+21_1307+32del