Canonical Allele Identifier: CA341171438

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103412500C>T (hg19) ; chr1:g.102946944C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102946944C>T , CM000663.2:g.102946944C>T	GRCh38
NC_000001.10:g.103412500C>T , CM000663.1:g.103412500C>T	GRCh37
NC_000001.9:g.103185088C>T	NCBI36
NG_008033.1:g.166553G>A
NG_008033.2:g.166553G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3181G>A MANE Select	ENSP00000359114.3:p.Glu1061Lys
ENST00000353414.8:c.3064G>A	ENSP00000302551.6:p.Glu1022Lys
ENST00000358392.6:c.3217G>A	ENSP00000351163.2:p.Glu1073Lys
ENST00000370096.7:c.3181G>A	ENSP00000359114.3:p.Glu1061Lys
ENST00000512756.5:c.2833G>A	ENSP00000426533.1:p.Glu945Lys
ENST00000635193.1:c.2515G>A
NM_001190709.1:c.3064G>A	NP_001177638.1:p.Glu1022Lys
NM_001854.3:c.3181G>A	NP_001845.3:p.Glu1061Lys
NM_080629.2:c.3217G>A	NP_542196.2:p.Glu1073Lys
NM_080630.3:c.2833G>A	NP_542197.3:p.Glu945Lys
XM_011540719.1:c.3181G>A	XP_011539021.1:p.Glu1061Lys
XM_011540720.1:c.1414G>A	XP_011539022.1:p.Glu472Lys
XM_011540721.1:c.769G>A	XP_011539023.1:p.Glu257Lys
NR_134980.1:n.3515G>A
XM_017000334.1:c.3334G>A	XP_016855823.1:p.Glu1112Lys
XM_017000335.1:c.3328G>A	XP_016855824.1:p.Glu1110Lys
XM_017000336.1:c.3334G>A	XP_016855825.1:p.Glu1112Lys
XM_017000337.1:c.1732G>A	XP_016855826.1:p.Glu578Lys
NM_001854.4:c.3181G>A MANE Select	NP_001845.3:p.Glu1061Lys
NM_080630.4:c.2833G>A	NP_542197.3:p.Glu945Lys
NR_134980.2:n.3541G>A
NM_001190709.2:c.3064G>A	NP_001177638.1:p.Glu1022Lys
NM_080629.3:c.3217G>A	NP_542196.2:p.Glu1073Lys