Canonical Allele Identifier: CA341171186
Gene: COL11A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.102946907A>T , CM000663.2:g.102946907A>T GRCh38
NC_000001.10:g.103412463A>T , CM000663.1:g.103412463A>T GRCh37
NC_000001.9:g.103185051A>T NCBI36
NG_008033.1:g.166590T>A
NG_008033.2:g.166590T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370096.9:c.3218T>A MANE Select ENSP00000359114.3:p.Leu1073Ter
ENST00000353414.8:c.3101T>A ENSP00000302551.6:p.Leu1034Ter
ENST00000358392.6:c.3254T>A ENSP00000351163.2:p.Leu1085Ter
ENST00000370096.7:c.3218T>A ENSP00000359114.3:p.Leu1073Ter
ENST00000512756.5:c.2870T>A ENSP00000426533.1:p.Leu957Ter
ENST00000635193.1:c.2552T>A
NM_001190709.1:c.3101T>A NP_001177638.1:p.Leu1034Ter
NM_001854.3:c.3218T>A NP_001845.3:p.Leu1073Ter
NM_080629.2:c.3254T>A NP_542196.2:p.Leu1085Ter
NM_080630.3:c.2870T>A NP_542197.3:p.Leu957Ter
XM_011540719.1:c.3218T>A XP_011539021.1:p.Leu1073Ter
XM_011540720.1:c.1451T>A XP_011539022.1:p.Leu484Ter
XM_011540721.1:c.806T>A XP_011539023.1:p.Leu269Ter
NR_134980.1:n.3552T>A
XM_017000334.1:c.3371T>A XP_016855823.1:p.Leu1124Ter
XM_017000335.1:c.3365T>A XP_016855824.1:p.Leu1122Ter
XM_017000336.1:c.3371T>A XP_016855825.1:p.Leu1124Ter
XM_017000337.1:c.1769T>A XP_016855826.1:p.Leu590Ter
NM_001854.4:c.3218T>A MANE Select NP_001845.3:p.Leu1073Ter
NM_080630.4:c.2870T>A NP_542197.3:p.Leu957Ter
NR_134980.2:n.3578T>A
NM_001190709.2:c.3101T>A NP_001177638.1:p.Leu1034Ter
NM_080629.3:c.3254T>A NP_542196.2:p.Leu1085Ter