Canonical Allele Identifier: CA1185271926
Gene: COL11A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.102978779T= , CM000663.2:g.102978779T= GRCh38
NC_000001.10:g.103444335T= , CM000663.1:g.103444335T= GRCh37
NC_000001.9:g.103216923T= NCBI36
NG_008033.1:g.134718A=
NG_008033.2:g.134718A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.2710-27A= MANE Select ENSP00000359114.3:n.2710-27A=
ENST00000353414.8:c.2593-27A= ENSP00000302551.6:n.2593-27A=
ENST00000358392.6:c.2746-27A= ENSP00000351163.2:n.2746-27A=
ENST00000370096.7:c.2710-27A= ENSP00000359114.3:n.2710-27A=
ENST00000512756.5:c.2362-27A= ENSP00000426533.1:n.2362-27A=
ENST00000635193.1:c.2044-27A=
NM_001190709.1:c.2593-27A= NP_001177638.1:n.2593-27A=
NM_001854.3:c.2710-27A= NP_001845.3:n.2710-27A=
NM_080629.2:c.2746-27A= NP_542196.2:n.2746-27A=
NM_080630.3:c.2362-27A= NP_542197.3:n.2362-27A=
XM_011540719.1:c.2710-27A= XP_011539021.1:n.2710-27A=
XM_011540720.1:c.943-27A= XP_011539022.1:n.943-27A=
XM_011540721.1:c.298-27A= XP_011539023.1:n.298-27A=
XR_946545.1:n.3124-27A=
NR_134980.1:n.3044-27A=
XM_017000334.1:c.2863-27A= XP_016855823.1:n.2863-27A=
XM_017000335.1:c.2857-27A= XP_016855824.1:n.2857-27A=
XM_017000336.1:c.2863-27A= XP_016855825.1:n.2863-27A=
XM_017000337.1:c.1261-27A= XP_016855826.1:n.1261-27A=
NM_001854.4:c.2710-27A= MANE Select NP_001845.3:n.2710-27A=
NM_080630.4:c.2362-27A= NP_542197.3:n.2362-27A=
NR_134980.2:n.3070-27A=
NM_001190709.2:c.2593-27A= NP_001177638.1:n.2593-27A=
NM_080629.3:c.2746-27A= NP_542196.2:n.2746-27A=