Canonical Allele Identifier: CA341163119
Gene: COL11A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.102978754T>C , CM000663.2:g.102978754T>C GRCh38
NC_000001.10:g.103444310T>C , CM000663.1:g.103444310T>C GRCh37
NC_000001.9:g.103216898T>C NCBI36
NG_008033.1:g.134743A>G
NG_008033.2:g.134743A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.2710-2A>G MANE Select ENSP00000359114.3:n.2710-2A>G
ENST00000353414.8:c.2593-2A>G ENSP00000302551.6:n.2593-2A>G
ENST00000358392.6:c.2746-2A>G ENSP00000351163.2:n.2746-2A>G
ENST00000370096.7:c.2710-2A>G ENSP00000359114.3:n.2710-2A>G
ENST00000512756.5:c.2362-2A>G ENSP00000426533.1:n.2362-2A>G
ENST00000635193.1:c.2044-2A>G
NM_001190709.1:c.2593-2A>G NP_001177638.1:n.2593-2A>G
NM_001854.3:c.2710-2A>G NP_001845.3:n.2710-2A>G
NM_080629.2:c.2746-2A>G NP_542196.2:n.2746-2A>G
NM_080630.3:c.2362-2A>G NP_542197.3:n.2362-2A>G
XM_011540719.1:c.2710-2A>G XP_011539021.1:n.2710-2A>G
XM_011540720.1:c.943-2A>G XP_011539022.1:n.943-2A>G
XM_011540721.1:c.298-2A>G XP_011539023.1:n.298-2A>G
XR_946545.1:n.3124-2A>G
NR_134980.1:n.3044-2A>G
XM_017000334.1:c.2863-2A>G XP_016855823.1:n.2863-2A>G
XM_017000335.1:c.2857-2A>G XP_016855824.1:n.2857-2A>G
XM_017000336.1:c.2863-2A>G XP_016855825.1:n.2863-2A>G
XM_017000337.1:c.1261-2A>G XP_016855826.1:n.1261-2A>G
NM_001854.4:c.2710-2A>G MANE Select NP_001845.3:n.2710-2A>G
NM_080630.4:c.2362-2A>G NP_542197.3:n.2362-2A>G
NR_134980.2:n.3070-2A>G
NM_001190709.2:c.2593-2A>G NP_001177638.1:n.2593-2A>G
NM_080629.3:c.2746-2A>G NP_542196.2:n.2746-2A>G