Canonical Allele Identifier: CA341175590

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103474063C>T (hg19) ; chr1:g.103008507C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103008507C>T , CM000663.2:g.103008507C>T	GRCh38
NC_000001.10:g.103474063C>T , CM000663.1:g.103474063C>T	GRCh37
NC_000001.9:g.103246651C>T	NCBI36
NG_008033.1:g.104990G>A
NG_008033.2:g.104990G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.1639G>A MANE Select	ENSP00000359114.3:p.Gly547Ser
ENST00000461720.6:c.1792G>A	ENSP00000494909.1:p.Gly598Ser
ENST00000644186.1:c.1639G>A	ENSP00000493821.1:p.Gly547Ser
ENST00000645458.1:c.1639G>A	ENSP00000494179.1:p.Gly547Ser
ENST00000647280.1:c.1639G>A	ENSP00000494583.1:p.Gly547Ser
ENST00000353414.8:c.1522G>A	ENSP00000302551.6:p.Gly508Ser
ENST00000358392.6:c.1675G>A	ENSP00000351163.2:p.Gly559Ser
ENST00000370096.7:c.1639G>A	ENSP00000359114.3:p.Gly547Ser
ENST00000427239.5:c.1675G>A	ENSP00000408640.1:p.Gly559Ser
ENST00000512756.5:c.1291G>A	ENSP00000426533.1:p.Gly431Ser
ENST00000635193.1:c.957G>A
NM_001190709.1:c.1522G>A	NP_001177638.1:p.Gly508Ser
NM_001854.3:c.1639G>A	NP_001845.3:p.Gly547Ser
NM_080629.2:c.1675G>A	NP_542196.2:p.Gly559Ser
NM_080630.3:c.1291G>A	NP_542197.3:p.Gly431Ser
XM_011540719.1:c.1639G>A	XP_011539021.1:p.Gly547Ser
XM_011540720.1:c.-85+169G>A	XP_011539022.1:n.-85+169G>A
XM_011540721.1:c.-790G>A	XP_011539023.1:n.-790G>A
XR_946545.1:n.2037G>A
NR_134980.1:n.1957G>A
XM_017000334.1:c.1792G>A	XP_016855823.1:p.Gly598Ser
XM_017000335.1:c.1786G>A	XP_016855824.1:p.Gly596Ser
XM_017000336.1:c.1792G>A	XP_016855825.1:p.Gly598Ser
XM_017000337.1:c.190G>A	XP_016855826.1:p.Gly64Ser
NM_001854.4:c.1639G>A MANE Select	NP_001845.3:p.Gly547Ser
NM_080630.4:c.1291G>A	NP_542197.3:p.Gly431Ser
NR_134980.2:n.1983G>A
NM_001190709.2:c.1522G>A	NP_001177638.1:p.Gly508Ser
NM_080629.3:c.1675G>A	NP_542196.2:p.Gly559Ser