Canonical Allele Identifier: CA689444472

Gene: COL2A1

Linked Data

• dbSNP Id: rs1217943692
• gnomAD v3: 12-47986149-TC-T
• gnomAD v4: 12-47986149-TC-T
• MyVariant Identifiers: chr12:g.48379933del (hg19) ; chr12:g.47986150del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47986150del , CM000674.2:g.47986150del	GRCh38
NC_000012.11:g.48379933del , CM000674.1:g.48379933del	GRCh37
NC_000012.10:g.46666200del	NCBI36
NG_008072.1:g.23353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337299.7:c.1321-185del	ENSP00000338213.6:n.1321-185del
ENST00000380518.8:c.1528-185del MANE Select	ENSP00000369889.3:n.1528-185del
ENST00000337299.6:c.1321-185del	ENSP00000338213.6:n.1321-185del
ENST00000380518.7:c.1528-185del	ENSP00000369889.3:n.1528-185del
ENST00000493991.5:n.452-185del
NM_001844.4:c.1528-185del	NP_001835.3:n.1528-185del
NM_033150.2:c.1321-185del	NP_149162.2:n.1321-185del
XM_006719242.2:c.1672-185del	XP_006719305.2:n.1672-185del
XM_011537928.1:c.1672-185del	XP_011536230.1:n.1672-185del
XM_011537929.1:c.1672-185del	XP_011536231.1:n.1672-185del
XM_011537930.1:c.1672-185del	XP_011536232.1:n.1672-185del
XM_011537931.1:c.1672-185del	XP_011536233.1:n.1672-185del
XM_011537932.1:c.1672-185del	XP_011536234.1:n.1672-185del
XM_011537933.1:c.1672-185del	XP_011536235.1:n.1672-185del
XM_011537934.1:c.1669-185del	XP_011536236.1:n.1669-185del
XM_011537935.1:c.616-185del	XP_011536237.1:n.616-185del
XM_017018828.1:c.1672-185del	XP_016874317.1:n.1672-185del
XM_017018829.1:c.1669-185del	XP_016874318.1:n.1669-185del
XM_017018830.1:c.1462-185del	XP_016874319.1:n.1462-185del
XM_017018831.2:c.982-185del	XP_016874320.1:n.982-185del
NM_001844.5:c.1528-185del MANE Select	NP_001835.3:n.1528-185del
NM_033150.3:c.1321-185del	NP_149162.2:n.1321-185del