Canonical Allele Identifier: CA2744832076
Gene: COL11A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.102978969_102978970insAGT , CM000663.2:g.102978969_102978970insAGT GRCh38
NC_000001.10:g.103444525_103444526insAGT , CM000663.1:g.103444525_103444526insAGT GRCh37
NC_000001.9:g.103217113_103217114insAGT NCBI36
NG_008033.1:g.134527_134528insACT
NG_008033.2:g.134527_134528insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.2656-57_2656-56insACT MANE Select ENSP00000359114.3:n.2656-57_2656-56insACT
ENST00000353414.8:c.2539-57_2539-56insACT ENSP00000302551.6:n.2539-57_2539-56insACT
ENST00000358392.6:c.2692-57_2692-56insACT ENSP00000351163.2:n.2692-57_2692-56insACT
ENST00000370096.7:c.2656-57_2656-56insACT ENSP00000359114.3:n.2656-57_2656-56insACT
ENST00000512756.5:c.2308-57_2308-56insACT ENSP00000426533.1:n.2308-57_2308-56insACT
ENST00000635193.1:c.1990-57_1990-56insACT
NM_001190709.1:c.2539-57_2539-56insACT NP_001177638.1:n.2539-57_2539-56insACT
NM_001854.3:c.2656-57_2656-56insACT NP_001845.3:n.2656-57_2656-56insACT
NM_080629.2:c.2692-57_2692-56insACT NP_542196.2:n.2692-57_2692-56insACT
NM_080630.3:c.2308-57_2308-56insACT NP_542197.3:n.2308-57_2308-56insACT
XM_011540719.1:c.2656-57_2656-56insACT XP_011539021.1:n.2656-57_2656-56insACT
XM_011540720.1:c.889-57_889-56insACT XP_011539022.1:n.889-57_889-56insACT
XM_011540721.1:c.244-57_244-56insACT XP_011539023.1:n.244-57_244-56insACT
XR_946545.1:n.3070-57_3070-56insACT
NR_134980.1:n.2990-57_2990-56insACT
XM_017000334.1:c.2809-57_2809-56insACT XP_016855823.1:n.2809-57_2809-56insACT
XM_017000335.1:c.2803-57_2803-56insACT XP_016855824.1:n.2803-57_2803-56insACT
XM_017000336.1:c.2809-57_2809-56insACT XP_016855825.1:n.2809-57_2809-56insACT
XM_017000337.1:c.1207-57_1207-56insACT XP_016855826.1:n.1207-57_1207-56insACT
NM_001854.4:c.2656-57_2656-56insACT MANE Select NP_001845.3:n.2656-57_2656-56insACT
NM_080630.4:c.2308-57_2308-56insACT NP_542197.3:n.2308-57_2308-56insACT
NR_134980.2:n.3016-57_3016-56insACT
NM_001190709.2:c.2539-57_2539-56insACT NP_001177638.1:n.2539-57_2539-56insACT
NM_080629.3:c.2692-57_2692-56insACT NP_542196.2:n.2692-57_2692-56insACT