Canonical Allele Identifier: CA783973432
Gene: COMP HGNC NCBI

Linked Data

dbSNP Id: rs1247140470
MyVariant Identifiers: chr19:g.18898725_18898726insTC (hg19) chr19:g.18787916_18787917insTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18787917_18787918insCT , CM000681.2:g.18787917_18787918insCT GRCh38
NC_000019.9:g.18898726_18898727insCT , CM000681.1:g.18898726_18898727insCT GRCh37
NC_000019.8:g.18759726_18759727insCT NCBI36
NG_007070.1:g.8389_8390insGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.976-267_976-266insGA MANE Select ENSP00000222271.2:n.976-267_976-266insGA
ENST00000222271.6:c.976-267_976-266insGA ENSP00000222271.2:n.976-267_976-266insGA
ENST00000425807.1:c.817-267_817-266insGA ENSP00000403792.1:n.817-267_817-266insGA
ENST00000542601.6:c.877-267_877-266insGA ENSP00000439156.2:n.877-267_877-266insGA
NM_000095.2:c.976-267_976-266insGA NP_000086.2:n.976-267_976-266insGA
NM_000095.3:c.976-267_976-266insGA MANE Select NP_000086.2:n.976-267_976-266insGA
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