Canonical Allele Identifier: CA341155562

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103025564C>G , CM000663.2:g.103025564C>G	GRCh38
NC_000001.10:g.103491120C>G , CM000663.1:g.103491120C>G	GRCh37
NC_000001.9:g.103263708C>G	NCBI36
NG_008033.1:g.87933G>C
NG_008033.2:g.87933G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.947G>C MANE Select	NP_001845.3:p.Ser316Thr
ENST00000370096.9:c.947G>C MANE Select	ENSP00000359114.3:p.Ser316Thr
NM_001190709.1:c.830G>C	NP_001177638.1:p.Ser277Thr
NM_001190709.2:c.830G>C	NP_001177638.1:p.Ser277Thr
NM_001854.3:c.947G>C	NP_001845.3:p.Ser316Thr
NM_080629.2:c.983G>C	NP_542196.2:p.Ser328Thr
NM_080629.3:c.983G>C	NP_542196.2:p.Ser328Thr
NM_080630.3:c.897+652G>C	NP_542197.3:n.897+652G>C
NM_080630.4:c.897+652G>C	NP_542197.3:n.897+652G>C
NR_134980.1:n.1265G>C
NR_134980.2:n.1291G>C
ENST00000353414.8:c.830G>C	ENSP00000302551.6:p.Ser277Thr
ENST00000358392.6:c.983G>C	ENSP00000351163.2:p.Ser328Thr
ENST00000370096.7:c.947G>C	ENSP00000359114.3:p.Ser316Thr
ENST00000427239.5:c.983G>C	ENSP00000408640.1:p.Ser328Thr
ENST00000461720.6:c.1100G>C	ENSP00000494909.1:p.Ser367Thr
ENST00000512756.5:c.897+652G>C	ENSP00000426533.1:n.897+652G>C
ENST00000635193.1:c.265G>C
ENST00000644186.1:c.947G>C	ENSP00000493821.1:p.Ser316Thr
ENST00000645458.1:c.947G>C	ENSP00000494179.1:p.Ser316Thr
ENST00000647280.1:c.947G>C	ENSP00000494583.1:p.Ser316Thr
XM_011540719.1:c.947G>C	XP_011539021.1:p.Ser316Thr
XM_011540721.1:c.-1482G>C	XP_011539023.1:n.-1482G>C
XM_017000334.1:c.1100G>C	XP_016855823.1:p.Ser367Thr
XM_017000335.1:c.1094G>C	XP_016855824.1:p.Ser365Thr
XM_017000336.1:c.1100G>C	XP_016855825.1:p.Ser367Thr
XR_946545.1:n.1345G>C