Canonical Allele Identifier: CA419200343

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444622A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979066A>C , CM000663.2:g.102979066A>C	GRCh38
NC_000001.10:g.103444622A>C , CM000663.1:g.103444622A>C	GRCh37
NC_000001.9:g.103217210A>C	NCBI36
NG_008033.1:g.134431T>G
NG_008033.2:g.134431T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2649T>G MANE Select	ENSP00000359114.3:p.Gly883=
ENST00000353414.8:c.2532T>G	ENSP00000302551.6:p.Gly844=
ENST00000358392.6:c.2685T>G	ENSP00000351163.2:p.Gly895=
ENST00000370096.7:c.2649T>G	ENSP00000359114.3:p.Gly883=
ENST00000512756.5:c.2301T>G	ENSP00000426533.1:p.Gly767=
ENST00000635193.1:c.1983T>G
NM_001190709.1:c.2532T>G	NP_001177638.1:p.Gly844=
NM_001854.3:c.2649T>G	NP_001845.3:p.Gly883=
NM_080629.2:c.2685T>G	NP_542196.2:p.Gly895=
NM_080630.3:c.2301T>G	NP_542197.3:p.Gly767=
XM_011540719.1:c.2649T>G	XP_011539021.1:p.Gly883=
XM_011540720.1:c.882T>G	XP_011539022.1:p.Gly294=
XM_011540721.1:c.237T>G	XP_011539023.1:p.Gly79=
XR_946545.1:n.3063T>G
NR_134980.1:n.2983T>G
XM_017000334.1:c.2802T>G	XP_016855823.1:p.Gly934=
XM_017000335.1:c.2796T>G	XP_016855824.1:p.Gly932=
XM_017000336.1:c.2802T>G	XP_016855825.1:p.Gly934=
XM_017000337.1:c.1200T>G	XP_016855826.1:p.Gly400=
NM_001854.4:c.2649T>G MANE Select	NP_001845.3:p.Gly883=
NM_080630.4:c.2301T>G	NP_542197.3:p.Gly767=
NR_134980.2:n.3009T>G
NM_001190709.2:c.2532T>G	NP_001177638.1:p.Gly844=
NM_080629.3:c.2685T>G	NP_542196.2:p.Gly895=