Canonical Allele Identifier: CA783973061

Gene: COMP

Linked Data

• dbSNP Id: rs1173356818
• MyVariant Identifiers: chr19:g.18898262_18898268del (hg19) ; chr19:g.18787453_18787459del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18787453_18787459del , CM000681.2:g.18787453_18787459del	GRCh38
NC_000019.9:g.18898262_18898268del , CM000681.1:g.18898262_18898268del	GRCh37
NC_000019.8:g.18759262_18759268del	NCBI36
NG_007070.1:g.8847_8853del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222271.7:c.1135+32_1135+38del MANE Select	ENSP00000222271.2:n.1135+32_1135+38del
ENST00000222271.6:c.1135+32_1135+38del	ENSP00000222271.2:n.1135+32_1135+38del
ENST00000425807.1:c.976+32_976+38del	ENSP00000403792.1:n.976+32_976+38del
ENST00000542601.6:c.1036+32_1036+38del	ENSP00000439156.2:n.1036+32_1036+38del
NM_000095.2:c.1135+32_1135+38del	NP_000086.2:n.1135+32_1135+38del
NM_000095.3:c.1135+32_1135+38del MANE Select	NP_000086.2:n.1135+32_1135+38del