Canonical Allele Identifier: CA27712489
Community Standard Title: NM_001854.4(COL11A1):c.948T>C (p.Ser316=)
Gene: COL11A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.103025563A>G , CM000663.2:g.103025563A>G GRCh38
NC_000001.10:g.103491119A>G , CM000663.1:g.103491119A>G GRCh37
NC_000001.9:g.103263707A>G NCBI36
NG_008033.1:g.87934T>C
NG_008033.2:g.87934T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001854.4:c.948T>C MANE Select NP_001845.3:p.Ser316=
ENST00000370096.9:c.948T>C MANE Select ENSP00000359114.3:p.Ser316=
NM_001190709.1:c.831T>C NP_001177638.1:p.Ser277=
NM_001190709.2:c.831T>C NP_001177638.1:p.Ser277=
NM_001854.3:c.948T>C NP_001845.3:p.Ser316=
NM_080629.2:c.984T>C NP_542196.2:p.Ser328=
NM_080629.3:c.984T>C NP_542196.2:p.Ser328=
NM_080630.3:c.897+653T>C NP_542197.3:n.897+653T>C
NM_080630.4:c.897+653T>C NP_542197.3:n.897+653T>C
NR_134980.1:n.1266T>C
NR_134980.2:n.1292T>C
ENST00000353414.8:c.831T>C ENSP00000302551.6:p.Ser277=
ENST00000358392.6:c.984T>C ENSP00000351163.2:p.Ser328=
ENST00000370096.7:c.948T>C ENSP00000359114.3:p.Ser316=
ENST00000427239.5:c.984T>C ENSP00000408640.1:p.Ser328=
ENST00000461720.6:c.1101T>C ENSP00000494909.1:p.Ser367=
ENST00000512756.5:c.897+653T>C ENSP00000426533.1:n.897+653T>C
ENST00000635193.1:c.266T>C
ENST00000644186.1:c.948T>C ENSP00000493821.1:p.Ser316=
ENST00000645458.1:c.948T>C ENSP00000494179.1:p.Ser316=
ENST00000647280.1:c.948T>C ENSP00000494583.1:p.Ser316=
XM_011540719.1:c.948T>C XP_011539021.1:p.Ser316=
XM_011540721.1:c.-1481T>C XP_011539023.1:n.-1481T>C
XM_017000334.1:c.1101T>C XP_016855823.1:p.Ser367=
XM_017000335.1:c.1095T>C XP_016855824.1:p.Ser365=
XM_017000336.1:c.1101T>C XP_016855825.1:p.Ser367=
XR_946545.1:n.1346T>C