Canonical Allele Identifier: CA341175465

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103474035C>A (hg19) ; chr1:g.103008479C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103008479C>A , CM000663.2:g.103008479C>A	GRCh38
NC_000001.10:g.103474035C>A , CM000663.1:g.103474035C>A	GRCh37
NC_000001.9:g.103246623C>A	NCBI36
NG_008033.1:g.105018G>T
NG_008033.2:g.105018G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.1667G>T MANE Select	ENSP00000359114.3:p.Gly556Val
ENST00000461720.6:c.1820G>T	ENSP00000494909.1:p.Gly607Val
ENST00000644186.1:c.1667G>T	ENSP00000493821.1:p.Gly556Val
ENST00000645458.1:c.1667G>T	ENSP00000494179.1:p.Gly556Val
ENST00000647280.1:c.1667G>T	ENSP00000494583.1:p.Gly556Val
ENST00000353414.8:c.1550G>T	ENSP00000302551.6:p.Gly517Val
ENST00000358392.6:c.1703G>T	ENSP00000351163.2:p.Gly568Val
ENST00000370096.7:c.1667G>T	ENSP00000359114.3:p.Gly556Val
ENST00000427239.5:c.1703G>T	ENSP00000408640.1:p.Gly568Val
ENST00000461720.5:n.15G>T
ENST00000512756.5:c.1319G>T	ENSP00000426533.1:p.Gly440Val
ENST00000635193.1:c.985G>T
NM_001190709.1:c.1550G>T	NP_001177638.1:p.Gly517Val
NM_001854.3:c.1667G>T	NP_001845.3:p.Gly556Val
NM_080629.2:c.1703G>T	NP_542196.2:p.Gly568Val
NM_080630.3:c.1319G>T	NP_542197.3:p.Gly440Val
XM_011540719.1:c.1667G>T	XP_011539021.1:p.Gly556Val
XM_011540720.1:c.-85+197G>T	XP_011539022.1:n.-85+197G>T
XM_011540721.1:c.-762G>T	XP_011539023.1:n.-762G>T
XR_946545.1:n.2065G>T
NR_134980.1:n.1985G>T
XM_017000334.1:c.1820G>T	XP_016855823.1:p.Gly607Val
XM_017000335.1:c.1814G>T	XP_016855824.1:p.Gly605Val
XM_017000336.1:c.1820G>T	XP_016855825.1:p.Gly607Val
XM_017000337.1:c.218G>T	XP_016855826.1:p.Gly73Val
NM_001854.4:c.1667G>T MANE Select	NP_001845.3:p.Gly556Val
NM_080630.4:c.1319G>T	NP_542197.3:p.Gly440Val
NR_134980.2:n.2011G>T
NM_001190709.2:c.1550G>T	NP_001177638.1:p.Gly517Val
NM_080629.3:c.1703G>T	NP_542196.2:p.Gly568Val