Canonical Allele Identifier: CA1185272014
Gene: COL11A1 HGNC NCBI

Linked Data

dbSNP Id: rs1662774485

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.102978953G>C , CM000663.2:g.102978953G>C GRCh38
NC_000001.10:g.103444509G>C , CM000663.1:g.103444509G>C GRCh37
NC_000001.9:g.103217097G>C NCBI36
NG_008033.1:g.134544C>G
NG_008033.2:g.134544C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.2656-40C>G MANE Select ENSP00000359114.3:n.2656-40C>G
ENST00000353414.8:c.2539-40C>G ENSP00000302551.6:n.2539-40C>G
ENST00000358392.6:c.2692-40C>G ENSP00000351163.2:n.2692-40C>G
ENST00000370096.7:c.2656-40C>G ENSP00000359114.3:n.2656-40C>G
ENST00000512756.5:c.2308-40C>G ENSP00000426533.1:n.2308-40C>G
ENST00000635193.1:c.1990-40C>G
NM_001190709.1:c.2539-40C>G NP_001177638.1:n.2539-40C>G
NM_001854.3:c.2656-40C>G NP_001845.3:n.2656-40C>G
NM_080629.2:c.2692-40C>G NP_542196.2:n.2692-40C>G
NM_080630.3:c.2308-40C>G NP_542197.3:n.2308-40C>G
XM_011540719.1:c.2656-40C>G XP_011539021.1:n.2656-40C>G
XM_011540720.1:c.889-40C>G XP_011539022.1:n.889-40C>G
XM_011540721.1:c.244-40C>G XP_011539023.1:n.244-40C>G
XR_946545.1:n.3070-40C>G
NR_134980.1:n.2990-40C>G
XM_017000334.1:c.2809-40C>G XP_016855823.1:n.2809-40C>G
XM_017000335.1:c.2803-40C>G XP_016855824.1:n.2803-40C>G
XM_017000336.1:c.2809-40C>G XP_016855825.1:n.2809-40C>G
XM_017000337.1:c.1207-40C>G XP_016855826.1:n.1207-40C>G
NM_001854.4:c.2656-40C>G MANE Select NP_001845.3:n.2656-40C>G
NM_080630.4:c.2308-40C>G NP_542197.3:n.2308-40C>G
NR_134980.2:n.3016-40C>G
NM_001190709.2:c.2539-40C>G NP_001177638.1:n.2539-40C>G
NM_080629.3:c.2692-40C>G NP_542196.2:n.2692-40C>G