Canonical Allele Identifier: CA341171435
Gene: COL11A1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.3181G>T MANE Select ENSP00000359114.3:p.Glu1061Ter
ENST00000353414.8:c.3064G>T ENSP00000302551.6:p.Glu1022Ter
ENST00000358392.6:c.3217G>T ENSP00000351163.2:p.Glu1073Ter
ENST00000370096.7:c.3181G>T ENSP00000359114.3:p.Glu1061Ter
ENST00000512756.5:c.2833G>T ENSP00000426533.1:p.Glu945Ter
ENST00000635193.1:c.2515G>T
NM_001190709.1:c.3064G>T NP_001177638.1:p.Glu1022Ter
NM_001854.3:c.3181G>T NP_001845.3:p.Glu1061Ter
NM_080629.2:c.3217G>T NP_542196.2:p.Glu1073Ter
NM_080630.3:c.2833G>T NP_542197.3:p.Glu945Ter
XM_011540719.1:c.3181G>T XP_011539021.1:p.Glu1061Ter
XM_011540720.1:c.1414G>T XP_011539022.1:p.Glu472Ter
XM_011540721.1:c.769G>T XP_011539023.1:p.Glu257Ter
NR_134980.1:n.3515G>T
XM_017000334.1:c.3334G>T XP_016855823.1:p.Glu1112Ter
XM_017000335.1:c.3328G>T XP_016855824.1:p.Glu1110Ter
XM_017000336.1:c.3334G>T XP_016855825.1:p.Glu1112Ter
XM_017000337.1:c.1732G>T XP_016855826.1:p.Glu578Ter
NM_001854.4:c.3181G>T MANE Select NP_001845.3:p.Glu1061Ter
NM_080630.4:c.2833G>T NP_542197.3:p.Glu945Ter
NR_134980.2:n.3541G>T
NM_001190709.2:c.3064G>T NP_001177638.1:p.Glu1022Ter
NM_080629.3:c.3217G>T NP_542196.2:p.Glu1073Ter