Canonical Allele Identifier: CA994237881
Gene: COMP HGNC NCBI

Linked Data

gnomAD v3: 19-18787882-C-CTTTT
gnomAD v4: 19-18787882-C-CTTTT
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787885_18787886insTTTT , CM000681.2:g.18787885_18787886insTTTT GRCh38
NC_000019.9:g.18898694_18898695insTTTT , CM000681.1:g.18898694_18898695insTTTT GRCh37
NC_000019.8:g.18759694_18759695insTTTT NCBI36
NG_007070.1:g.8423_8424insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-233_976-232insAAAA MANE Select ENSP00000222271.2:n.976-233_976-232insAAAA
ENST00000222271.6:c.976-233_976-232insAAAA ENSP00000222271.2:n.976-233_976-232insAAAA
ENST00000425807.1:c.817-233_817-232insAAAA ENSP00000403792.1:n.817-233_817-232insAAAA
ENST00000542601.6:c.877-233_877-232insAAAA ENSP00000439156.2:n.877-233_877-232insAAAA
NM_000095.2:c.976-233_976-232insAAAA NP_000086.2:n.976-233_976-232insAAAA
NM_000095.3:c.976-233_976-232insAAAA MANE Select NP_000086.2:n.976-233_976-232insAAAA
Search 100 bp 5'
Search 100 bp 3'