Canonical Allele Identifier: CA1144228916

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102989562C= , CM000663.2:g.102989562C=	GRCh38
NC_000001.10:g.103455118C= , CM000663.1:g.103455118C=	GRCh37
NC_000001.9:g.103227706C=	NCBI36
NG_008033.1:g.123935G=
NG_008033.2:g.123935G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.2350G= MANE Select	NP_001845.3:p.Gly784=
ENST00000370096.9:c.2350G= MANE Select	ENSP00000359114.3:p.Gly784=
NM_001190709.1:c.2233G=	NP_001177638.1:p.Gly745=
NM_001190709.2:c.2233G=	NP_001177638.1:p.Gly745=
NM_001854.3:c.2350G=	NP_001845.3:p.Gly784=
NM_080629.2:c.2386G=	NP_542196.2:p.Gly796=
NM_080629.3:c.2386G=	NP_542196.2:p.Gly796=
NM_080630.3:c.2002G=	NP_542197.3:p.Gly668=
NM_080630.4:c.2002G=	NP_542197.3:p.Gly668=
NR_134980.1:n.2668G=
NR_134980.2:n.2694G=
ENST00000353414.8:c.2233G=	ENSP00000302551.6:p.Gly745=
ENST00000358392.6:c.2386G=	ENSP00000351163.2:p.Gly796=
ENST00000370096.7:c.2350G=	ENSP00000359114.3:p.Gly784=
ENST00000512756.5:c.2002G=	ENSP00000426533.1:p.Gly668=
ENST00000635193.1:c.1668G=
XM_011540719.1:c.2350G=	XP_011539021.1:p.Gly784=
XM_011540720.1:c.583G=	XP_011539022.1:p.Gly195=
XM_011540721.1:c.-79G=	XP_011539023.1:n.-79G=
XM_017000334.1:c.2503G=	XP_016855823.1:p.Gly835=
XM_017000335.1:c.2497G=	XP_016855824.1:p.Gly833=
XM_017000336.1:c.2503G=	XP_016855825.1:p.Gly835=
XM_017000337.1:c.901G=	XP_016855826.1:p.Gly301=
XR_946545.1:n.2748G=