Canonical Allele Identifier: CA419200210

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444434A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978878A>T , CM000663.2:g.102978878A>T	GRCh38
NC_000001.10:g.103444434A>T , CM000663.1:g.103444434A>T	GRCh37
NC_000001.9:g.103217022A>T	NCBI36
NG_008033.1:g.134619T>A
NG_008033.2:g.134619T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2691T>A MANE Select	ENSP00000359114.3:p.Thr897=
ENST00000353414.8:c.2574T>A	ENSP00000302551.6:p.Thr858=
ENST00000358392.6:c.2727T>A	ENSP00000351163.2:p.Thr909=
ENST00000370096.7:c.2691T>A	ENSP00000359114.3:p.Thr897=
ENST00000512756.5:c.2343T>A	ENSP00000426533.1:p.Thr781=
ENST00000635193.1:c.2025T>A
NM_001190709.1:c.2574T>A	NP_001177638.1:p.Thr858=
NM_001854.3:c.2691T>A	NP_001845.3:p.Thr897=
NM_080629.2:c.2727T>A	NP_542196.2:p.Thr909=
NM_080630.3:c.2343T>A	NP_542197.3:p.Thr781=
XM_011540719.1:c.2691T>A	XP_011539021.1:p.Thr897=
XM_011540720.1:c.924T>A	XP_011539022.1:p.Thr308=
XM_011540721.1:c.279T>A	XP_011539023.1:p.Thr93=
XR_946545.1:n.3105T>A
NR_134980.1:n.3025T>A
XM_017000334.1:c.2844T>A	XP_016855823.1:p.Thr948=
XM_017000335.1:c.2838T>A	XP_016855824.1:p.Thr946=
XM_017000336.1:c.2844T>A	XP_016855825.1:p.Thr948=
XM_017000337.1:c.1242T>A	XP_016855826.1:p.Thr414=
NM_001854.4:c.2691T>A MANE Select	NP_001845.3:p.Thr897=
NM_080630.4:c.2343T>A	NP_542197.3:p.Thr781=
NR_134980.2:n.3051T>A
NM_001190709.2:c.2574T>A	NP_001177638.1:p.Thr858=
NM_080629.3:c.2727T>A	NP_542196.2:p.Thr909=