Canonical Allele Identifier: CA341155576

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103025570A>C , CM000663.2:g.103025570A>C	GRCh38
NC_000001.10:g.103491126A>C , CM000663.1:g.103491126A>C	GRCh37
NC_000001.9:g.103263714A>C	NCBI36
NG_008033.1:g.87927T>G
NG_008033.2:g.87927T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.941T>G MANE Select	NP_001845.3:p.Met314Arg
ENST00000370096.9:c.941T>G MANE Select	ENSP00000359114.3:p.Met314Arg
NM_001190709.1:c.824T>G	NP_001177638.1:p.Met275Arg
NM_001190709.2:c.824T>G	NP_001177638.1:p.Met275Arg
NM_001854.3:c.941T>G	NP_001845.3:p.Met314Arg
NM_080629.2:c.977T>G	NP_542196.2:p.Met326Arg
NM_080629.3:c.977T>G	NP_542196.2:p.Met326Arg
NM_080630.3:c.897+646T>G	NP_542197.3:n.897+646T>G
NM_080630.4:c.897+646T>G	NP_542197.3:n.897+646T>G
NR_134980.1:n.1259T>G
NR_134980.2:n.1285T>G
ENST00000353414.8:c.824T>G	ENSP00000302551.6:p.Met275Arg
ENST00000358392.6:c.977T>G	ENSP00000351163.2:p.Met326Arg
ENST00000370096.7:c.941T>G	ENSP00000359114.3:p.Met314Arg
ENST00000427239.5:c.977T>G	ENSP00000408640.1:p.Met326Arg
ENST00000461720.6:c.1094T>G	ENSP00000494909.1:p.Met365Arg
ENST00000512756.5:c.897+646T>G	ENSP00000426533.1:n.897+646T>G
ENST00000635193.1:c.259T>G
ENST00000644186.1:c.941T>G	ENSP00000493821.1:p.Met314Arg
ENST00000645458.1:c.941T>G	ENSP00000494179.1:p.Met314Arg
ENST00000647280.1:c.941T>G	ENSP00000494583.1:p.Met314Arg
XM_011540719.1:c.941T>G	XP_011539021.1:p.Met314Arg
XM_011540721.1:c.-1488T>G	XP_011539023.1:n.-1488T>G
XM_017000334.1:c.1094T>G	XP_016855823.1:p.Met365Arg
XM_017000335.1:c.1088T>G	XP_016855824.1:p.Met363Arg
XM_017000336.1:c.1094T>G	XP_016855825.1:p.Met365Arg
XR_946545.1:n.1339T>G