Canonical Allele Identifier: CA974111
Gene: COL11A1 HGNC NCBI

Linked Data

dbSNP Id: rs773986853

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.102946987T>C , CM000663.2:g.102946987T>C GRCh38
NC_000001.10:g.103412543T>C , CM000663.1:g.103412543T>C GRCh37
NC_000001.9:g.103185131T>C NCBI36
NG_008033.1:g.166510A>G
NG_008033.2:g.166510A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.3169-31A>G MANE Select ENSP00000359114.3:n.3169-31A>G
ENST00000353414.8:c.3052-31A>G ENSP00000302551.6:n.3052-31A>G
ENST00000358392.6:c.3205-31A>G ENSP00000351163.2:n.3205-31A>G
ENST00000370096.7:c.3169-31A>G ENSP00000359114.3:n.3169-31A>G
ENST00000512756.5:c.2821-31A>G ENSP00000426533.1:n.2821-31A>G
ENST00000635193.1:c.2503-31A>G
NM_001190709.1:c.3052-31A>G NP_001177638.1:n.3052-31A>G
NM_001854.3:c.3169-31A>G NP_001845.3:n.3169-31A>G
NM_080629.2:c.3205-31A>G NP_542196.2:n.3205-31A>G
NM_080630.3:c.2821-31A>G NP_542197.3:n.2821-31A>G
XM_011540719.1:c.3169-31A>G XP_011539021.1:n.3169-31A>G
XM_011540720.1:c.1402-31A>G XP_011539022.1:n.1402-31A>G
XM_011540721.1:c.757-31A>G XP_011539023.1:n.757-31A>G
NR_134980.1:n.3503-31A>G
XM_017000334.1:c.3322-31A>G XP_016855823.1:n.3322-31A>G
XM_017000335.1:c.3316-31A>G XP_016855824.1:n.3316-31A>G
XM_017000336.1:c.3322-31A>G XP_016855825.1:n.3322-31A>G
XM_017000337.1:c.1720-31A>G XP_016855826.1:n.1720-31A>G
NM_001854.4:c.3169-31A>G MANE Select NP_001845.3:n.3169-31A>G
NM_080630.4:c.2821-31A>G NP_542197.3:n.2821-31A>G
NR_134980.2:n.3529-31A>G
NM_001190709.2:c.3052-31A>G NP_001177638.1:n.3052-31A>G
NM_080629.3:c.3205-31A>G NP_542196.2:n.3205-31A>G