Canonical Allele Identifier: CA341155501

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103025546G>T , CM000663.2:g.103025546G>T	GRCh38
NC_000001.10:g.103491102G>T , CM000663.1:g.103491102G>T	GRCh37
NC_000001.9:g.103263690G>T	NCBI36
NG_008033.1:g.87951C>A
NG_008033.2:g.87951C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.965C>A MANE Select	NP_001845.3:p.Pro322His
ENST00000370096.9:c.965C>A MANE Select	ENSP00000359114.3:p.Pro322His
NM_001190709.1:c.848C>A	NP_001177638.1:p.Pro283His
NM_001190709.2:c.848C>A	NP_001177638.1:p.Pro283His
NM_001854.3:c.965C>A	NP_001845.3:p.Pro322His
NM_080629.2:c.1001C>A	NP_542196.2:p.Pro334His
NM_080629.3:c.1001C>A	NP_542196.2:p.Pro334His
NM_080630.3:c.897+670C>A	NP_542197.3:n.897+670C>A
NM_080630.4:c.897+670C>A	NP_542197.3:n.897+670C>A
NR_134980.1:n.1283C>A
NR_134980.2:n.1309C>A
ENST00000353414.8:c.848C>A	ENSP00000302551.6:p.Pro283His
ENST00000358392.6:c.1001C>A	ENSP00000351163.2:p.Pro334His
ENST00000370096.7:c.965C>A	ENSP00000359114.3:p.Pro322His
ENST00000427239.5:c.1001C>A	ENSP00000408640.1:p.Pro334His
ENST00000461720.6:c.1118C>A	ENSP00000494909.1:p.Pro373His
ENST00000512756.5:c.897+670C>A	ENSP00000426533.1:n.897+670C>A
ENST00000635193.1:c.283C>A
ENST00000644186.1:c.965C>A	ENSP00000493821.1:p.Pro322His
ENST00000645458.1:c.965C>A	ENSP00000494179.1:p.Pro322His
ENST00000647280.1:c.965C>A	ENSP00000494583.1:p.Pro322His
XM_011540719.1:c.965C>A	XP_011539021.1:p.Pro322His
XM_011540721.1:c.-1464C>A	XP_011539023.1:n.-1464C>A
XM_017000334.1:c.1118C>A	XP_016855823.1:p.Pro373His
XM_017000335.1:c.1112C>A	XP_016855824.1:p.Pro371His
XM_017000336.1:c.1118C>A	XP_016855825.1:p.Pro373His
XR_946545.1:n.1363C>A