Canonical Allele Identifier: CA341155634
Community Standard Title: NM_001854.4(COL11A1):c.923A>C (p.Glu308Ala)
Gene: COL11A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.103025588T>G , CM000663.2:g.103025588T>G GRCh38
NC_000001.10:g.103491144T>G , CM000663.1:g.103491144T>G GRCh37
NC_000001.9:g.103263732T>G NCBI36
NG_008033.1:g.87909A>C
NG_008033.2:g.87909A>C

Transcript Alleles

HGVS Amino-acid Change
NM_001854.4:c.923A>C MANE Select NP_001845.3:p.Glu308Ala
ENST00000370096.9:c.923A>C MANE Select ENSP00000359114.3:p.Glu308Ala
NM_001190709.1:c.806A>C NP_001177638.1:p.Glu269Ala
NM_001190709.2:c.806A>C NP_001177638.1:p.Glu269Ala
NM_001854.3:c.923A>C NP_001845.3:p.Glu308Ala
NM_080629.2:c.959A>C NP_542196.2:p.Glu320Ala
NM_080629.3:c.959A>C NP_542196.2:p.Glu320Ala
NM_080630.3:c.897+628A>C NP_542197.3:n.897+628A>C
NM_080630.4:c.897+628A>C NP_542197.3:n.897+628A>C
NR_134980.1:n.1241A>C
NR_134980.2:n.1267A>C
ENST00000353414.8:c.806A>C ENSP00000302551.6:p.Glu269Ala
ENST00000358392.6:c.959A>C ENSP00000351163.2:p.Glu320Ala
ENST00000370096.7:c.923A>C ENSP00000359114.3:p.Glu308Ala
ENST00000427239.5:c.959A>C ENSP00000408640.1:p.Glu320Ala
ENST00000461720.6:c.1076A>C ENSP00000494909.1:p.Glu359Ala
ENST00000512756.5:c.897+628A>C ENSP00000426533.1:n.897+628A>C
ENST00000635193.1:c.241A>C
ENST00000644186.1:c.923A>C ENSP00000493821.1:p.Glu308Ala
ENST00000645458.1:c.923A>C ENSP00000494179.1:p.Glu308Ala
ENST00000647280.1:c.923A>C ENSP00000494583.1:p.Glu308Ala
XM_011540719.1:c.923A>C XP_011539021.1:p.Glu308Ala
XM_011540721.1:c.-1506A>C XP_011539023.1:n.-1506A>C
XM_017000334.1:c.1076A>C XP_016855823.1:p.Glu359Ala
XM_017000335.1:c.1070A>C XP_016855824.1:p.Glu357Ala
XM_017000336.1:c.1076A>C XP_016855825.1:p.Glu359Ala
XR_946545.1:n.1321A>C