Canonical Allele Identifier: CA341170136

Gene: COL11A1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102998312G>T , CM000663.2:g.102998312G>T	GRCh38
NC_000001.10:g.103463868G>T , CM000663.1:g.103463868G>T	GRCh37
NC_000001.9:g.103236456G>T	NCBI36
NG_008033.1:g.115185C>A
NG_008033.2:g.115185C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2194C>A MANE Select	ENSP00000359114.3:p.Pro732Thr
ENST00000353414.8:c.2077C>A	ENSP00000302551.6:p.Pro693Thr
ENST00000358392.6:c.2230C>A	ENSP00000351163.2:p.Pro744Thr
ENST00000370096.7:c.2194C>A	ENSP00000359114.3:p.Pro732Thr
ENST00000512756.5:c.1846C>A	ENSP00000426533.1:p.Pro616Thr
ENST00000635193.1:c.1512C>A
NM_001190709.1:c.2077C>A	NP_001177638.1:p.Pro693Thr
NM_001854.3:c.2194C>A	NP_001845.3:p.Pro732Thr
NM_080629.2:c.2230C>A	NP_542196.2:p.Pro744Thr
NM_080630.3:c.1846C>A	NP_542197.3:p.Pro616Thr
XM_011540719.1:c.2194C>A	XP_011539021.1:p.Pro732Thr
XM_011540720.1:c.427C>A	XP_011539022.1:p.Pro143Thr
XM_011540721.1:c.-235C>A	XP_011539023.1:n.-235C>A
XR_946545.1:n.2592C>A
NR_134980.1:n.2512C>A
XM_017000334.1:c.2347C>A	XP_016855823.1:p.Pro783Thr
XM_017000335.1:c.2341C>A	XP_016855824.1:p.Pro781Thr
XM_017000336.1:c.2347C>A	XP_016855825.1:p.Pro783Thr
XM_017000337.1:c.745C>A	XP_016855826.1:p.Pro249Thr
NM_001854.4:c.2194C>A MANE Select	NP_001845.3:p.Pro732Thr
NM_080630.4:c.1846C>A	NP_542197.3:p.Pro616Thr
NR_134980.2:n.2538C>A
NM_001190709.2:c.2077C>A	NP_001177638.1:p.Pro693Thr
NM_080629.3:c.2230C>A	NP_542196.2:p.Pro744Thr