Canonical Allele Identifier: CA2646806423
Gene: COL11A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.102998237T>C , CM000663.2:g.102998237T>C GRCh38
NC_000001.10:g.103463793T>C , CM000663.1:g.103463793T>C GRCh37
NC_000001.9:g.103236381T>C NCBI36
NG_008033.1:g.115260A>G
NG_008033.2:g.115260A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.2196+73A>G MANE Select ENSP00000359114.3:n.2196+73A>G
ENST00000353414.8:c.2079+73A>G ENSP00000302551.6:n.2079+73A>G
ENST00000358392.6:c.2232+73A>G ENSP00000351163.2:n.2232+73A>G
ENST00000370096.7:c.2196+73A>G ENSP00000359114.3:n.2196+73A>G
ENST00000512756.5:c.1848+73A>G ENSP00000426533.1:n.1848+73A>G
ENST00000635193.1:c.1514+73A>G
NM_001190709.1:c.2079+73A>G NP_001177638.1:n.2079+73A>G
NM_001854.3:c.2196+73A>G NP_001845.3:n.2196+73A>G
NM_080629.2:c.2232+73A>G NP_542196.2:n.2232+73A>G
NM_080630.3:c.1848+73A>G NP_542197.3:n.1848+73A>G
XM_011540719.1:c.2196+73A>G XP_011539021.1:n.2196+73A>G
XM_011540720.1:c.429+73A>G XP_011539022.1:n.429+73A>G
XM_011540721.1:c.-233+73A>G XP_011539023.1:n.-233+73A>G
XR_946545.1:n.2594+73A>G
NR_134980.1:n.2514+73A>G
XM_017000334.1:c.2349+73A>G XP_016855823.1:n.2349+73A>G
XM_017000335.1:c.2343+73A>G XP_016855824.1:n.2343+73A>G
XM_017000336.1:c.2349+73A>G XP_016855825.1:n.2349+73A>G
XM_017000337.1:c.747+73A>G XP_016855826.1:n.747+73A>G
NM_001854.4:c.2196+73A>G MANE Select NP_001845.3:n.2196+73A>G
NM_080630.4:c.1848+73A>G NP_542197.3:n.1848+73A>G
NR_134980.2:n.2540+73A>G
NM_001190709.2:c.2079+73A>G NP_001177638.1:n.2079+73A>G
NM_080629.3:c.2232+73A>G NP_542196.2:n.2232+73A>G