Canonical Allele Identifier: CA2744833822
Gene: COL11A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.103008577_103008581del , CM000663.2:g.103008577_103008581del GRCh38
NC_000001.10:g.103474133_103474137del , CM000663.1:g.103474133_103474137del GRCh37
NC_000001.9:g.103246721_103246725del NCBI36
NG_008033.1:g.104916_104920del
NG_008033.2:g.104916_104920del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.1630-65_1630-61del MANE Select ENSP00000359114.3:n.1630-65_1630-61del
ENST00000461720.6:c.1783-65_1783-61del ENSP00000494909.1:n.1783-65_1783-61del
ENST00000644186.1:c.1630-65_1630-61del ENSP00000493821.1:n.1630-65_1630-61del
ENST00000645458.1:c.1630-65_1630-61del ENSP00000494179.1:n.1630-65_1630-61del
ENST00000647280.1:c.1630-65_1630-61del ENSP00000494583.1:n.1630-65_1630-61del
ENST00000353414.8:c.1513-65_1513-61del ENSP00000302551.6:n.1513-65_1513-61del
ENST00000358392.6:c.1666-65_1666-61del ENSP00000351163.2:n.1666-65_1666-61del
ENST00000370096.7:c.1630-65_1630-61del ENSP00000359114.3:n.1630-65_1630-61del
ENST00000427239.5:c.1666-65_1666-61del ENSP00000408640.1:n.1666-65_1666-61del
ENST00000512756.5:c.1282-65_1282-61del ENSP00000426533.1:n.1282-65_1282-61del
ENST00000635193.1:c.948-65_948-61del
NM_001190709.1:c.1513-65_1513-61del NP_001177638.1:n.1513-65_1513-61del
NM_001854.3:c.1630-65_1630-61del NP_001845.3:n.1630-65_1630-61del
NM_080629.2:c.1666-65_1666-61del NP_542196.2:n.1666-65_1666-61del
NM_080630.3:c.1282-65_1282-61del NP_542197.3:n.1282-65_1282-61del
XM_011540719.1:c.1630-65_1630-61del XP_011539021.1:n.1630-65_1630-61del
XM_011540720.1:c.-85+95_-85+99del XP_011539022.1:n.-85+95_-85+99del
XM_011540721.1:c.-799-65_-799-61del XP_011539023.1:n.-799-65_-799-61del
XR_946545.1:n.2028-65_2028-61del
NR_134980.1:n.1948-65_1948-61del
XM_017000334.1:c.1783-65_1783-61del XP_016855823.1:n.1783-65_1783-61del
XM_017000335.1:c.1777-65_1777-61del XP_016855824.1:n.1777-65_1777-61del
XM_017000336.1:c.1783-65_1783-61del XP_016855825.1:n.1783-65_1783-61del
XM_017000337.1:c.181-65_181-61del XP_016855826.1:n.181-65_181-61del
NM_001854.4:c.1630-65_1630-61del MANE Select NP_001845.3:n.1630-65_1630-61del
NM_080630.4:c.1282-65_1282-61del NP_542197.3:n.1282-65_1282-61del
NR_134980.2:n.1974-65_1974-61del
NM_001190709.2:c.1513-65_1513-61del NP_001177638.1:n.1513-65_1513-61del
NM_080629.3:c.1666-65_1666-61del NP_542196.2:n.1666-65_1666-61del