Canonical Allele Identifier: CA419197340
Community Standard Title: NM_001854.4(COL11A1):c.960A>G (p.Glu320=)
Gene: COL11A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.103025551T>C , CM000663.2:g.103025551T>C GRCh38
NC_000001.10:g.103491107T>C , CM000663.1:g.103491107T>C GRCh37
NC_000001.9:g.103263695T>C NCBI36
NG_008033.1:g.87946A>G
NG_008033.2:g.87946A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001854.4:c.960A>G MANE Select NP_001845.3:p.Glu320=
ENST00000370096.9:c.960A>G MANE Select ENSP00000359114.3:p.Glu320=
NM_001190709.1:c.843A>G NP_001177638.1:p.Glu281=
NM_001190709.2:c.843A>G NP_001177638.1:p.Glu281=
NM_001854.3:c.960A>G NP_001845.3:p.Glu320=
NM_080629.2:c.996A>G NP_542196.2:p.Glu332=
NM_080629.3:c.996A>G NP_542196.2:p.Glu332=
NM_080630.3:c.897+665A>G NP_542197.3:n.897+665A>G
NM_080630.4:c.897+665A>G NP_542197.3:n.897+665A>G
NR_134980.1:n.1278A>G
NR_134980.2:n.1304A>G
ENST00000353414.8:c.843A>G ENSP00000302551.6:p.Glu281=
ENST00000358392.6:c.996A>G ENSP00000351163.2:p.Glu332=
ENST00000370096.7:c.960A>G ENSP00000359114.3:p.Glu320=
ENST00000427239.5:c.996A>G ENSP00000408640.1:p.Glu332=
ENST00000461720.6:c.1113A>G ENSP00000494909.1:p.Glu371=
ENST00000512756.5:c.897+665A>G ENSP00000426533.1:n.897+665A>G
ENST00000635193.1:c.278A>G
ENST00000644186.1:c.960A>G ENSP00000493821.1:p.Glu320=
ENST00000645458.1:c.960A>G ENSP00000494179.1:p.Glu320=
ENST00000647280.1:c.960A>G ENSP00000494583.1:p.Glu320=
XM_011540719.1:c.960A>G XP_011539021.1:p.Glu320=
XM_011540721.1:c.-1469A>G XP_011539023.1:n.-1469A>G
XM_017000334.1:c.1113A>G XP_016855823.1:p.Glu371=
XM_017000335.1:c.1107A>G XP_016855824.1:p.Glu369=
XM_017000336.1:c.1113A>G XP_016855825.1:p.Glu371=
XR_946545.1:n.1358A>G