Canonical Allele Identifier: CA1185292181

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103025547G= , CM000663.2:g.103025547G=	GRCh38
NC_000001.10:g.103491103G= , CM000663.1:g.103491103G=	GRCh37
NC_000001.9:g.103263691G=	NCBI36
NG_008033.1:g.87950C=
NG_008033.2:g.87950C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.964C= MANE Select	NP_001845.3:p.Pro322=
ENST00000370096.9:c.964C= MANE Select	ENSP00000359114.3:p.Pro322=
NM_001190709.1:c.847C=	NP_001177638.1:p.Pro283=
NM_001190709.2:c.847C=	NP_001177638.1:p.Pro283=
NM_001854.3:c.964C=	NP_001845.3:p.Pro322=
NM_080629.2:c.1000C=	NP_542196.2:p.Pro334=
NM_080629.3:c.1000C=	NP_542196.2:p.Pro334=
NM_080630.3:c.897+669C=	NP_542197.3:n.897+669C=
NM_080630.4:c.897+669C=	NP_542197.3:n.897+669C=
NR_134980.1:n.1282C=
NR_134980.2:n.1308C=
ENST00000353414.8:c.847C=	ENSP00000302551.6:p.Pro283=
ENST00000358392.6:c.1000C=	ENSP00000351163.2:p.Pro334=
ENST00000370096.7:c.964C=	ENSP00000359114.3:p.Pro322=
ENST00000427239.5:c.1000C=	ENSP00000408640.1:p.Pro334=
ENST00000461720.6:c.1117C=	ENSP00000494909.1:p.Pro373=
ENST00000512756.5:c.897+669C=	ENSP00000426533.1:n.897+669C=
ENST00000635193.1:c.282C=
ENST00000644186.1:c.964C=	ENSP00000493821.1:p.Pro322=
ENST00000645458.1:c.964C=	ENSP00000494179.1:p.Pro322=
ENST00000647280.1:c.964C=	ENSP00000494583.1:p.Pro322=
XM_011540719.1:c.964C=	XP_011539021.1:p.Pro322=
XM_011540721.1:c.-1465C=	XP_011539023.1:n.-1465C=
XM_017000334.1:c.1117C=	XP_016855823.1:p.Pro373=
XM_017000335.1:c.1111C=	XP_016855824.1:p.Pro371=
XM_017000336.1:c.1117C=	XP_016855825.1:p.Pro373=
XR_946545.1:n.1362C=