Canonical Allele Identifier: CA2646803985
Gene: COL11A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.102961953C>A , CM000663.2:g.102961953C>A GRCh38
NC_000001.10:g.103427509C>A , CM000663.1:g.103427509C>A GRCh37
NC_000001.9:g.103200097C>A NCBI36
NG_008033.1:g.151544G>T
NG_008033.2:g.151544G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.3115-34G>T MANE Select ENSP00000359114.3:n.3115-34G>T
ENST00000353414.8:c.2998-34G>T ENSP00000302551.6:n.2998-34G>T
ENST00000358392.6:c.3151-34G>T ENSP00000351163.2:n.3151-34G>T
ENST00000370096.7:c.3115-34G>T ENSP00000359114.3:n.3115-34G>T
ENST00000465209.1:n.123-34G>T
ENST00000512756.5:c.2767-34G>T ENSP00000426533.1:n.2767-34G>T
ENST00000635193.1:c.2449-34G>T
NM_001190709.1:c.2998-34G>T NP_001177638.1:n.2998-34G>T
NM_001854.3:c.3115-34G>T NP_001845.3:n.3115-34G>T
NM_080629.2:c.3151-34G>T NP_542196.2:n.3151-34G>T
NM_080630.3:c.2767-34G>T NP_542197.3:n.2767-34G>T
XM_011540719.1:c.3115-34G>T XP_011539021.1:n.3115-34G>T
XM_011540720.1:c.1348-34G>T XP_011539022.1:n.1348-34G>T
XM_011540721.1:c.703-34G>T XP_011539023.1:n.703-34G>T
NR_134980.1:n.3449-34G>T
XM_017000334.1:c.3268-34G>T XP_016855823.1:n.3268-34G>T
XM_017000335.1:c.3262-34G>T XP_016855824.1:n.3262-34G>T
XM_017000336.1:c.3268-34G>T XP_016855825.1:n.3268-34G>T
XM_017000337.1:c.1666-34G>T XP_016855826.1:n.1666-34G>T
NM_001854.4:c.3115-34G>T MANE Select NP_001845.3:n.3115-34G>T
NM_080630.4:c.2767-34G>T NP_542197.3:n.2767-34G>T
NR_134980.2:n.3475-34G>T
NM_001190709.2:c.2998-34G>T NP_001177638.1:n.2998-34G>T
NM_080629.3:c.3151-34G>T NP_542196.2:n.3151-34G>T