Canonical Allele Identifier: CA783973378
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs764518645
MyVariant Identifiers: chr19:g.18898679_18898680insTTTTTT (hg19) chr19:g.18787870_18787871insTTTTTT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787873_18787874insTTTTTT , CM000681.2:g.18787873_18787874insTTTTTT GRCh38
NC_000019.9:g.18898682_18898683insTTTTTT , CM000681.1:g.18898682_18898683insTTTTTT GRCh37
NC_000019.8:g.18759682_18759683insTTTTTT NCBI36
NG_007070.1:g.8435_8436insAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-221_976-220insAAAAAA MANE Select ENSP00000222271.2:n.976-221_976-220insAAAAAA
ENST00000222271.6:c.976-221_976-220insAAAAAA ENSP00000222271.2:n.976-221_976-220insAAAAAA
ENST00000425807.1:c.817-221_817-220insAAAAAA ENSP00000403792.1:n.817-221_817-220insAAAAAA
ENST00000542601.6:c.877-221_877-220insAAAAAA ENSP00000439156.2:n.877-221_877-220insAAAAAA
NM_000095.2:c.976-221_976-220insAAAAAA NP_000086.2:n.976-221_976-220insAAAAAA
NM_000095.3:c.976-221_976-220insAAAAAA MANE Select NP_000086.2:n.976-221_976-220insAAAAAA
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