Canonical Allele Identifier: CA2580060736

Gene: COL11A1

Linked Data

• ClinVar Variation Id: 2082908
• ClinVar RCV Id: RCV002999497

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103008447A>C , CM000663.2:g.103008447A>C	GRCh38
NC_000001.10:g.103474003A>C , CM000663.1:g.103474003A>C	GRCh37
NC_000001.9:g.103246591A>C	NCBI36
NG_008033.1:g.105050T>G
NG_008033.2:g.105050T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370096.9:c.1683+16T>G MANE Select	ENSP00000359114.3:n.1683+16T>G
ENST00000461720.6:c.1836+16T>G	ENSP00000494909.1:n.1836+16T>G
ENST00000644186.1:c.1683+16T>G	ENSP00000493821.1:n.1683+16T>G
ENST00000645458.1:c.1683+16T>G	ENSP00000494179.1:n.1683+16T>G
ENST00000647280.1:c.1683+16T>G	ENSP00000494583.1:n.1683+16T>G
ENST00000353414.8:c.1566+16T>G	ENSP00000302551.6:n.1566+16T>G
ENST00000358392.6:c.1719+16T>G	ENSP00000351163.2:n.1719+16T>G
ENST00000370096.7:c.1683+16T>G	ENSP00000359114.3:n.1683+16T>G
ENST00000461720.5:n.31+16T>G
ENST00000512756.5:c.1335+16T>G	ENSP00000426533.1:n.1335+16T>G
ENST00000635193.1:c.1001+16T>G
NM_001190709.1:c.1566+16T>G	NP_001177638.1:n.1566+16T>G
NM_001854.3:c.1683+16T>G	NP_001845.3:n.1683+16T>G
NM_080629.2:c.1719+16T>G	NP_542196.2:n.1719+16T>G
NM_080630.3:c.1335+16T>G	NP_542197.3:n.1335+16T>G
XM_011540719.1:c.1683+16T>G	XP_011539021.1:n.1683+16T>G
XM_011540720.1:c.-85+229T>G	XP_011539022.1:n.-85+229T>G
XM_011540721.1:c.-746+16T>G	XP_011539023.1:n.-746+16T>G
XR_946545.1:n.2081+16T>G
NR_134980.1:n.2001+16T>G
XM_017000334.1:c.1836+16T>G	XP_016855823.1:n.1836+16T>G
XM_017000335.1:c.1830+16T>G	XP_016855824.1:n.1830+16T>G
XM_017000336.1:c.1836+16T>G	XP_016855825.1:n.1836+16T>G
XM_017000337.1:c.234+16T>G	XP_016855826.1:n.234+16T>G
NM_001854.4:c.1683+16T>G MANE Select	NP_001845.3:n.1683+16T>G
NM_080630.4:c.1335+16T>G	NP_542197.3:n.1335+16T>G
NR_134980.2:n.2027+16T>G
NM_001190709.2:c.1566+16T>G	NP_001177638.1:n.1566+16T>G
NM_080629.3:c.1719+16T>G	NP_542196.2:n.1719+16T>G