Canonical Allele Identifier: CA1185284692

Gene: COL11A1

Linked Data

• dbSNP Id: rs1665834342

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103008541_103008542insGGGTGATTCAAGATATAGTAG , CM000663.2:g.103008541_103008542insGGGTGATTCAAGATATAGTAG	GRCh38
NC_000001.10:g.103474097_103474098insGGGTGATTCAAGATATAGTAG , CM000663.1:g.103474097_103474098insGGGTGATTCAAGATATAGTAG	GRCh37
NC_000001.9:g.103246685_103246686insGGGTGATTCAAGATATAGTAG	NCBI36
NG_008033.1:g.104955_104956insCTACTATATCTTGAATCACCC
NG_008033.2:g.104955_104956insCTACTATATCTTGAATCACCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000370096.9:c.1630-26_1630-25insCTACTATATCTTGAATCACCC MANE Select	ENSP00000359114.3:n.1630-26_1630-25insCTA...
ENST00000461720.6:c.1783-26_1783-25insCTACTATATCTTGAATCACCC	ENSP00000494909.1:n.1783-26_1783-25insCTA...
ENST00000644186.1:c.1630-26_1630-25insCTACTATATCTTGAATCACCC	ENSP00000493821.1:n.1630-26_1630-25insCTA...
ENST00000645458.1:c.1630-26_1630-25insCTACTATATCTTGAATCACCC	ENSP00000494179.1:n.1630-26_1630-25insCTA...
ENST00000647280.1:c.1630-26_1630-25insCTACTATATCTTGAATCACCC	ENSP00000494583.1:n.1630-26_1630-25insCTA...
ENST00000353414.8:c.1513-26_1513-25insCTACTATATCTTGAATCACCC	ENSP00000302551.6:n.1513-26_1513-25insCTA...
ENST00000358392.6:c.1666-26_1666-25insCTACTATATCTTGAATCACCC	ENSP00000351163.2:n.1666-26_1666-25insCTA...
ENST00000370096.7:c.1630-26_1630-25insCTACTATATCTTGAATCACCC	ENSP00000359114.3:n.1630-26_1630-25insCTA...
ENST00000427239.5:c.1666-26_1666-25insCTACTATATCTTGAATCACCC	ENSP00000408640.1:n.1666-26_1666-25insCTA...
ENST00000512756.5:c.1282-26_1282-25insCTACTATATCTTGAATCACCC	ENSP00000426533.1:n.1282-26_1282-25insCTA...
ENST00000635193.1:c.948-26_948-25insCTACTATATCTTGAATCACCC
NM_001190709.1:c.1513-26_1513-25insCTACTATATCTTGAATCACCC	NP_001177638.1:n.1513-26_1513-25insCTACTA...
NM_001854.3:c.1630-26_1630-25insCTACTATATCTTGAATCACCC	NP_001845.3:n.1630-26_1630-25insCTACTATAT...
NM_080629.2:c.1666-26_1666-25insCTACTATATCTTGAATCACCC	NP_542196.2:n.1666-26_1666-25insCTACTATAT...
NM_080630.3:c.1282-26_1282-25insCTACTATATCTTGAATCACCC	NP_542197.3:n.1282-26_1282-25insCTACTATAT...
XM_011540719.1:c.1630-26_1630-25insCTACTATATCTTGAATCACCC	XP_011539021.1:n.1630-26_1630-25insCTACTA...
XM_011540720.1:c.-85+134_-85+135insCTACTATATCTTGAATCACCC	XP_011539022.1:n.-85+134_-85+135insCTACTA...
XM_011540721.1:c.-799-26_-799-25insCTACTATATCTTGAATCACCC	XP_011539023.1:n.-799-26_-799-25insCTACTA...
XR_946545.1:n.2028-26_2028-25insCTACTATATCTTGAATCACCC
NR_134980.1:n.1948-26_1948-25insCTACTATATCTTGAATCACCC
XM_017000334.1:c.1783-26_1783-25insCTACTATATCTTGAATCACCC	XP_016855823.1:n.1783-26_1783-25insCTACTA...
XM_017000335.1:c.1777-26_1777-25insCTACTATATCTTGAATCACCC	XP_016855824.1:n.1777-26_1777-25insCTACTA...
XM_017000336.1:c.1783-26_1783-25insCTACTATATCTTGAATCACCC	XP_016855825.1:n.1783-26_1783-25insCTACTA...
XM_017000337.1:c.181-26_181-25insCTACTATATCTTGAATCACCC	XP_016855826.1:n.181-26_181-25insCTACTATA...
NM_001854.4:c.1630-26_1630-25insCTACTATATCTTGAATCACCC MANE Select	NP_001845.3:n.1630-26_1630-25insCTACTATAT...
NM_080630.4:c.1282-26_1282-25insCTACTATATCTTGAATCACCC	NP_542197.3:n.1282-26_1282-25insCTACTATAT...
NR_134980.2:n.1974-26_1974-25insCTACTATATCTTGAATCACCC
NM_001190709.2:c.1513-26_1513-25insCTACTATATCTTGAATCACCC	NP_001177638.1:n.1513-26_1513-25insCTACTA...
NM_080629.3:c.1666-26_1666-25insCTACTATATCTTGAATCACCC	NP_542196.2:n.1666-26_1666-25insCTACTATAT...