Canonical Allele Identifier: CA2646808304
Gene: COL11A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.103008524G>A , CM000663.2:g.103008524G>A GRCh38
NC_000001.10:g.103474080G>A , CM000663.1:g.103474080G>A GRCh37
NC_000001.9:g.103246668G>A NCBI36
NG_008033.1:g.104973C>T
NG_008033.2:g.104973C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370096.9:c.1630-8C>T MANE Select ENSP00000359114.3:n.1630-8C>T
ENST00000461720.6:c.1783-8C>T ENSP00000494909.1:n.1783-8C>T
ENST00000644186.1:c.1630-8C>T ENSP00000493821.1:n.1630-8C>T
ENST00000645458.1:c.1630-8C>T ENSP00000494179.1:n.1630-8C>T
ENST00000647280.1:c.1630-8C>T ENSP00000494583.1:n.1630-8C>T
ENST00000353414.8:c.1513-8C>T ENSP00000302551.6:n.1513-8C>T
ENST00000358392.6:c.1666-8C>T ENSP00000351163.2:n.1666-8C>T
ENST00000370096.7:c.1630-8C>T ENSP00000359114.3:n.1630-8C>T
ENST00000427239.5:c.1666-8C>T ENSP00000408640.1:n.1666-8C>T
ENST00000512756.5:c.1282-8C>T ENSP00000426533.1:n.1282-8C>T
ENST00000635193.1:c.948-8C>T
NM_001190709.1:c.1513-8C>T NP_001177638.1:n.1513-8C>T
NM_001854.3:c.1630-8C>T NP_001845.3:n.1630-8C>T
NM_080629.2:c.1666-8C>T NP_542196.2:n.1666-8C>T
NM_080630.3:c.1282-8C>T NP_542197.3:n.1282-8C>T
XM_011540719.1:c.1630-8C>T XP_011539021.1:n.1630-8C>T
XM_011540720.1:c.-85+152C>T XP_011539022.1:n.-85+152C>T
XM_011540721.1:c.-799-8C>T XP_011539023.1:n.-799-8C>T
XR_946545.1:n.2028-8C>T
NR_134980.1:n.1948-8C>T
XM_017000334.1:c.1783-8C>T XP_016855823.1:n.1783-8C>T
XM_017000335.1:c.1777-8C>T XP_016855824.1:n.1777-8C>T
XM_017000336.1:c.1783-8C>T XP_016855825.1:n.1783-8C>T
XM_017000337.1:c.181-8C>T XP_016855826.1:n.181-8C>T
NM_001854.4:c.1630-8C>T MANE Select NP_001845.3:n.1630-8C>T
NM_080630.4:c.1282-8C>T NP_542197.3:n.1282-8C>T
NR_134980.2:n.1974-8C>T
NM_001190709.2:c.1513-8C>T NP_001177638.1:n.1513-8C>T
NM_080629.3:c.1666-8C>T NP_542196.2:n.1666-8C>T