Canonical Allele Identifier: CA341170186

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102998324C>T , CM000663.2:g.102998324C>T	GRCh38
NC_000001.10:g.103463880C>T , CM000663.1:g.103463880C>T	GRCh37
NC_000001.9:g.103236468C>T	NCBI36
NG_008033.1:g.115173G>A
NG_008033.2:g.115173G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.2182G>A MANE Select	NP_001845.3:p.Ala728Thr
ENST00000370096.9:c.2182G>A MANE Select	ENSP00000359114.3:p.Ala728Thr
NM_001190709.1:c.2065G>A	NP_001177638.1:p.Ala689Thr
NM_001190709.2:c.2065G>A	NP_001177638.1:p.Ala689Thr
NM_001854.3:c.2182G>A	NP_001845.3:p.Ala728Thr
NM_080629.2:c.2218G>A	NP_542196.2:p.Ala740Thr
NM_080629.3:c.2218G>A	NP_542196.2:p.Ala740Thr
NM_080630.3:c.1834G>A	NP_542197.3:p.Ala612Thr
NM_080630.4:c.1834G>A	NP_542197.3:p.Ala612Thr
NR_134980.1:n.2500G>A
NR_134980.2:n.2526G>A
ENST00000353414.8:c.2065G>A	ENSP00000302551.6:p.Ala689Thr
ENST00000358392.6:c.2218G>A	ENSP00000351163.2:p.Ala740Thr
ENST00000370096.7:c.2182G>A	ENSP00000359114.3:p.Ala728Thr
ENST00000512756.5:c.1834G>A	ENSP00000426533.1:p.Ala612Thr
ENST00000635193.1:c.1500G>A
XM_011540719.1:c.2182G>A	XP_011539021.1:p.Ala728Thr
XM_011540720.1:c.415G>A	XP_011539022.1:p.Ala139Thr
XM_011540721.1:c.-247G>A	XP_011539023.1:n.-247G>A
XM_017000334.1:c.2335G>A	XP_016855823.1:p.Ala779Thr
XM_017000335.1:c.2329G>A	XP_016855824.1:p.Ala777Thr
XM_017000336.1:c.2335G>A	XP_016855825.1:p.Ala779Thr
XM_017000337.1:c.733G>A	XP_016855826.1:p.Ala245Thr
XR_946545.1:n.2580G>A