Canonical Allele Identifier: CA341163734

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444651C>T (hg19) ; chr1:g.102979095C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979095C>T , CM000663.2:g.102979095C>T	GRCh38
NC_000001.10:g.103444651C>T , CM000663.1:g.103444651C>T	GRCh37
NC_000001.9:g.103217239C>T	NCBI36
NG_008033.1:g.134402G>A
NG_008033.2:g.134402G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2620G>A MANE Select	ENSP00000359114.3:p.Gly874Ser
ENST00000353414.8:c.2503G>A	ENSP00000302551.6:p.Gly835Ser
ENST00000358392.6:c.2656G>A	ENSP00000351163.2:p.Gly886Ser
ENST00000370096.7:c.2620G>A	ENSP00000359114.3:p.Gly874Ser
ENST00000512756.5:c.2272G>A	ENSP00000426533.1:p.Gly758Ser
ENST00000635193.1:c.1954G>A
NM_001190709.1:c.2503G>A	NP_001177638.1:p.Gly835Ser
NM_001854.3:c.2620G>A	NP_001845.3:p.Gly874Ser
NM_080629.2:c.2656G>A	NP_542196.2:p.Gly886Ser
NM_080630.3:c.2272G>A	NP_542197.3:p.Gly758Ser
XM_011540719.1:c.2620G>A	XP_011539021.1:p.Gly874Ser
XM_011540720.1:c.853G>A	XP_011539022.1:p.Gly285Ser
XM_011540721.1:c.208G>A	XP_011539023.1:p.Gly70Ser
XR_946545.1:n.3034G>A
NR_134980.1:n.2954G>A
XM_017000334.1:c.2773G>A	XP_016855823.1:p.Gly925Ser
XM_017000335.1:c.2767G>A	XP_016855824.1:p.Gly923Ser
XM_017000336.1:c.2773G>A	XP_016855825.1:p.Gly925Ser
XM_017000337.1:c.1171G>A	XP_016855826.1:p.Gly391Ser
NM_001854.4:c.2620G>A MANE Select	NP_001845.3:p.Gly874Ser
NM_080630.4:c.2272G>A	NP_542197.3:p.Gly758Ser
NR_134980.2:n.2980G>A
NM_001190709.2:c.2503G>A	NP_001177638.1:p.Gly835Ser
NM_080629.3:c.2656G>A	NP_542196.2:p.Gly886Ser