Canonical Allele Identifier: CA341162990

Gene: COL11A1

Linked Data

• COSMIC: COSM6120272 ; COSM6120273
• MyVariant Identifiers: chr1:g.103444295C>A (hg19) ; chr1:g.102978739C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978739C>A , CM000663.2:g.102978739C>A	GRCh38
NC_000001.10:g.103444295C>A , CM000663.1:g.103444295C>A	GRCh37
NC_000001.9:g.103216883C>A	NCBI36
NG_008033.1:g.134758G>T
NG_008033.2:g.134758G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2723G>T MANE Select	ENSP00000359114.3:p.Gly908Val
ENST00000353414.8:c.2606G>T	ENSP00000302551.6:p.Gly869Val
ENST00000358392.6:c.2759G>T	ENSP00000351163.2:p.Gly920Val
ENST00000370096.7:c.2723G>T	ENSP00000359114.3:p.Gly908Val
ENST00000512756.5:c.2375G>T	ENSP00000426533.1:p.Gly792Val
ENST00000635193.1:c.2057G>T
NM_001190709.1:c.2606G>T	NP_001177638.1:p.Gly869Val
NM_001854.3:c.2723G>T	NP_001845.3:p.Gly908Val
NM_080629.2:c.2759G>T	NP_542196.2:p.Gly920Val
NM_080630.3:c.2375G>T	NP_542197.3:p.Gly792Val
XM_011540719.1:c.2723G>T	XP_011539021.1:p.Gly908Val
XM_011540720.1:c.956G>T	XP_011539022.1:p.Gly319Val
XM_011540721.1:c.311G>T	XP_011539023.1:p.Gly104Val
XR_946545.1:n.3137G>T
NR_134980.1:n.3057G>T
XM_017000334.1:c.2876G>T	XP_016855823.1:p.Gly959Val
XM_017000335.1:c.2870G>T	XP_016855824.1:p.Gly957Val
XM_017000336.1:c.2876G>T	XP_016855825.1:p.Gly959Val
XM_017000337.1:c.1274G>T	XP_016855826.1:p.Gly425Val
NM_001854.4:c.2723G>T MANE Select	NP_001845.3:p.Gly908Val
NM_080630.4:c.2375G>T	NP_542197.3:p.Gly792Val
NR_134980.2:n.3083G>T
NM_001190709.2:c.2606G>T	NP_001177638.1:p.Gly869Val
NM_080629.3:c.2759G>T	NP_542196.2:p.Gly920Val