Canonical Allele Identifier: CA419199982

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444297A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978741A>C , CM000663.2:g.102978741A>C	GRCh38
NC_000001.10:g.103444297A>C , CM000663.1:g.103444297A>C	GRCh37
NC_000001.9:g.103216885A>C	NCBI36
NG_008033.1:g.134756T>G
NG_008033.2:g.134756T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2721T>G MANE Select	ENSP00000359114.3:p.Gly907=
ENST00000353414.8:c.2604T>G	ENSP00000302551.6:p.Gly868=
ENST00000358392.6:c.2757T>G	ENSP00000351163.2:p.Gly919=
ENST00000370096.7:c.2721T>G	ENSP00000359114.3:p.Gly907=
ENST00000512756.5:c.2373T>G	ENSP00000426533.1:p.Gly791=
ENST00000635193.1:c.2055T>G
NM_001190709.1:c.2604T>G	NP_001177638.1:p.Gly868=
NM_001854.3:c.2721T>G	NP_001845.3:p.Gly907=
NM_080629.2:c.2757T>G	NP_542196.2:p.Gly919=
NM_080630.3:c.2373T>G	NP_542197.3:p.Gly791=
XM_011540719.1:c.2721T>G	XP_011539021.1:p.Gly907=
XM_011540720.1:c.954T>G	XP_011539022.1:p.Gly318=
XM_011540721.1:c.309T>G	XP_011539023.1:p.Gly103=
XR_946545.1:n.3135T>G
NR_134980.1:n.3055T>G
XM_017000334.1:c.2874T>G	XP_016855823.1:p.Gly958=
XM_017000335.1:c.2868T>G	XP_016855824.1:p.Gly956=
XM_017000336.1:c.2874T>G	XP_016855825.1:p.Gly958=
XM_017000337.1:c.1272T>G	XP_016855826.1:p.Gly424=
NM_001854.4:c.2721T>G MANE Select	NP_001845.3:p.Gly907=
NM_080630.4:c.2373T>G	NP_542197.3:p.Gly791=
NR_134980.2:n.3081T>G
NM_001190709.2:c.2604T>G	NP_001177638.1:p.Gly868=
NM_080629.3:c.2757T>G	NP_542196.2:p.Gly919=