Canonical Allele Identifier: CA341162915

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444278G>T (hg19) ; chr1:g.102978722G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978722G>T , CM000663.2:g.102978722G>T	GRCh38
NC_000001.10:g.103444278G>T , CM000663.1:g.103444278G>T	GRCh37
NC_000001.9:g.103216866G>T	NCBI36
NG_008033.1:g.134775C>A
NG_008033.2:g.134775C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2740C>A MANE Select	ENSP00000359114.3:p.Pro914Thr
ENST00000353414.8:c.2623C>A	ENSP00000302551.6:p.Pro875Thr
ENST00000358392.6:c.2776C>A	ENSP00000351163.2:p.Pro926Thr
ENST00000370096.7:c.2740C>A	ENSP00000359114.3:p.Pro914Thr
ENST00000512756.5:c.2392C>A	ENSP00000426533.1:p.Pro798Thr
ENST00000635193.1:c.2074C>A
NM_001190709.1:c.2623C>A	NP_001177638.1:p.Pro875Thr
NM_001854.3:c.2740C>A	NP_001845.3:p.Pro914Thr
NM_080629.2:c.2776C>A	NP_542196.2:p.Pro926Thr
NM_080630.3:c.2392C>A	NP_542197.3:p.Pro798Thr
XM_011540719.1:c.2740C>A	XP_011539021.1:p.Pro914Thr
XM_011540720.1:c.973C>A	XP_011539022.1:p.Pro325Thr
XM_011540721.1:c.328C>A	XP_011539023.1:p.Pro110Thr
XR_946545.1:n.3154C>A
NR_134980.1:n.3074C>A
XM_017000334.1:c.2893C>A	XP_016855823.1:p.Pro965Thr
XM_017000335.1:c.2887C>A	XP_016855824.1:p.Pro963Thr
XM_017000336.1:c.2893C>A	XP_016855825.1:p.Pro965Thr
XM_017000337.1:c.1291C>A	XP_016855826.1:p.Pro431Thr
NM_001854.4:c.2740C>A MANE Select	NP_001845.3:p.Pro914Thr
NM_080630.4:c.2392C>A	NP_542197.3:p.Pro798Thr
NR_134980.2:n.3100C>A
NM_001190709.2:c.2623C>A	NP_001177638.1:p.Pro875Thr
NM_080629.3:c.2776C>A	NP_542196.2:p.Pro926Thr