Canonical Allele Identifier: CA341163398
Gene: COL11A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.102978901A>C , CM000663.2:g.102978901A>C GRCh38
NC_000001.10:g.103444457A>C , CM000663.1:g.103444457A>C GRCh37
NC_000001.9:g.103217045A>C NCBI36
NG_008033.1:g.134596T>G
NG_008033.2:g.134596T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.2668T>G MANE Select ENSP00000359114.3:p.Ser890Ala
ENST00000353414.8:c.2551T>G ENSP00000302551.6:p.Ser851Ala
ENST00000358392.6:c.2704T>G ENSP00000351163.2:p.Ser902Ala
ENST00000370096.7:c.2668T>G ENSP00000359114.3:p.Ser890Ala
ENST00000512756.5:c.2320T>G ENSP00000426533.1:p.Ser774Ala
ENST00000635193.1:c.2002T>G
NM_001190709.1:c.2551T>G NP_001177638.1:p.Ser851Ala
NM_001854.3:c.2668T>G NP_001845.3:p.Ser890Ala
NM_080629.2:c.2704T>G NP_542196.2:p.Ser902Ala
NM_080630.3:c.2320T>G NP_542197.3:p.Ser774Ala
XM_011540719.1:c.2668T>G XP_011539021.1:p.Ser890Ala
XM_011540720.1:c.901T>G XP_011539022.1:p.Ser301Ala
XM_011540721.1:c.256T>G XP_011539023.1:p.Ser86Ala
XR_946545.1:n.3082T>G
NR_134980.1:n.3002T>G
XM_017000334.1:c.2821T>G XP_016855823.1:p.Ser941Ala
XM_017000335.1:c.2815T>G XP_016855824.1:p.Ser939Ala
XM_017000336.1:c.2821T>G XP_016855825.1:p.Ser941Ala
XM_017000337.1:c.1219T>G XP_016855826.1:p.Ser407Ala
NM_001854.4:c.2668T>G MANE Select NP_001845.3:p.Ser890Ala
NM_080630.4:c.2320T>G NP_542197.3:p.Ser774Ala
NR_134980.2:n.3028T>G
NM_001190709.2:c.2551T>G NP_001177638.1:p.Ser851Ala
NM_080629.3:c.2704T>G NP_542196.2:p.Ser902Ala