Canonical Allele Identifier: CA419205532

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103412483A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102946927A>C , CM000663.2:g.102946927A>C	GRCh38
NC_000001.10:g.103412483A>C , CM000663.1:g.103412483A>C	GRCh37
NC_000001.9:g.103185071A>C	NCBI36
NG_008033.1:g.166570T>G
NG_008033.2:g.166570T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3198T>G MANE Select	ENSP00000359114.3:p.Gly1066=
ENST00000353414.8:c.3081T>G	ENSP00000302551.6:p.Gly1027=
ENST00000358392.6:c.3234T>G	ENSP00000351163.2:p.Gly1078=
ENST00000370096.7:c.3198T>G	ENSP00000359114.3:p.Gly1066=
ENST00000512756.5:c.2850T>G	ENSP00000426533.1:p.Gly950=
ENST00000635193.1:c.2532T>G
NM_001190709.1:c.3081T>G	NP_001177638.1:p.Gly1027=
NM_001854.3:c.3198T>G	NP_001845.3:p.Gly1066=
NM_080629.2:c.3234T>G	NP_542196.2:p.Gly1078=
NM_080630.3:c.2850T>G	NP_542197.3:p.Gly950=
XM_011540719.1:c.3198T>G	XP_011539021.1:p.Gly1066=
XM_011540720.1:c.1431T>G	XP_011539022.1:p.Gly477=
XM_011540721.1:c.786T>G	XP_011539023.1:p.Gly262=
NR_134980.1:n.3532T>G
XM_017000334.1:c.3351T>G	XP_016855823.1:p.Gly1117=
XM_017000335.1:c.3345T>G	XP_016855824.1:p.Gly1115=
XM_017000336.1:c.3351T>G	XP_016855825.1:p.Gly1117=
XM_017000337.1:c.1749T>G	XP_016855826.1:p.Gly583=
NM_001854.4:c.3198T>G MANE Select	NP_001845.3:p.Gly1066=
NM_080630.4:c.2850T>G	NP_542197.3:p.Gly950=
NR_134980.2:n.3558T>G
NM_001190709.2:c.3081T>G	NP_001177638.1:p.Gly1027=
NM_080629.3:c.3234T>G	NP_542196.2:p.Gly1078=