Canonical Allele Identifier: CA341155648

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103025591T>C , CM000663.2:g.103025591T>C	GRCh38
NC_000001.10:g.103491147T>C , CM000663.1:g.103491147T>C	GRCh37
NC_000001.9:g.103263735T>C	NCBI36
NG_008033.1:g.87906A>G
NG_008033.2:g.87906A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.920A>G MANE Select	NP_001845.3:p.Gln307Arg
ENST00000370096.9:c.920A>G MANE Select	ENSP00000359114.3:p.Gln307Arg
NM_001190709.1:c.803A>G	NP_001177638.1:p.Gln268Arg
NM_001190709.2:c.803A>G	NP_001177638.1:p.Gln268Arg
NM_001854.3:c.920A>G	NP_001845.3:p.Gln307Arg
NM_080629.2:c.956A>G	NP_542196.2:p.Gln319Arg
NM_080629.3:c.956A>G	NP_542196.2:p.Gln319Arg
NM_080630.3:c.897+625A>G	NP_542197.3:n.897+625A>G
NM_080630.4:c.897+625A>G	NP_542197.3:n.897+625A>G
NR_134980.1:n.1238A>G
NR_134980.2:n.1264A>G
ENST00000353414.8:c.803A>G	ENSP00000302551.6:p.Gln268Arg
ENST00000358392.6:c.956A>G	ENSP00000351163.2:p.Gln319Arg
ENST00000370096.7:c.920A>G	ENSP00000359114.3:p.Gln307Arg
ENST00000427239.5:c.956A>G	ENSP00000408640.1:p.Gln319Arg
ENST00000461720.6:c.1073A>G	ENSP00000494909.1:p.Gln358Arg
ENST00000512756.5:c.897+625A>G	ENSP00000426533.1:n.897+625A>G
ENST00000635193.1:c.238A>G
ENST00000644186.1:c.920A>G	ENSP00000493821.1:p.Gln307Arg
ENST00000645458.1:c.920A>G	ENSP00000494179.1:p.Gln307Arg
ENST00000647280.1:c.920A>G	ENSP00000494583.1:p.Gln307Arg
XM_011540719.1:c.920A>G	XP_011539021.1:p.Gln307Arg
XM_011540721.1:c.-1509A>G	XP_011539023.1:n.-1509A>G
XM_017000334.1:c.1073A>G	XP_016855823.1:p.Gln358Arg
XM_017000335.1:c.1067A>G	XP_016855824.1:p.Gln356Arg
XM_017000336.1:c.1073A>G	XP_016855825.1:p.Gln358Arg
XR_946545.1:n.1318A>G