Canonical Allele Identifier: CA973305

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102879863G>T , CM000663.2:g.102879863G>T	GRCh38
NC_000001.10:g.103345419G>T , CM000663.1:g.103345419G>T	GRCh37
NC_000001.9:g.103118007G>T	NCBI36
NG_008033.1:g.233634C>A
NG_008033.2:g.233634C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.5094C>A MANE Select	NP_001845.3:p.Phe1698Leu
ENST00000370096.9:c.5094C>A MANE Select	ENSP00000359114.3:p.Phe1698Leu
NM_001190709.1:c.4977C>A	NP_001177638.1:p.Phe1659Leu
NM_001190709.2:c.4977C>A	NP_001177638.1:p.Phe1659Leu
NM_001854.3:c.5094C>A	NP_001845.3:p.Phe1698Leu
NM_080629.2:c.5130C>A	NP_542196.2:p.Phe1710Leu
NM_080629.3:c.5130C>A	NP_542196.2:p.Phe1710Leu
NM_080630.3:c.4746C>A	NP_542197.3:p.Phe1582Leu
NM_080630.4:c.4746C>A	NP_542197.3:p.Phe1582Leu
NR_134980.1:n.5428C>A
NR_134980.2:n.5454C>A
ENST00000353414.8:c.4977C>A	ENSP00000302551.6:p.Phe1659Leu
ENST00000358392.6:c.5130C>A	ENSP00000351163.2:p.Phe1710Leu
ENST00000370096.7:c.5094C>A	ENSP00000359114.3:p.Phe1698Leu
ENST00000470170.1:n.156C>A
ENST00000512756.5:c.4746C>A	ENSP00000426533.1:p.Phe1582Leu
ENST00000635193.1:c.4428C>A
ENST00000639098.1:n.467C>A
XM_011540720.1:c.3327C>A	XP_011539022.1:p.Phe1109Leu
XM_011540721.1:c.2682C>A	XP_011539023.1:p.Phe894Leu
XM_017000334.1:c.5247C>A	XP_016855823.1:p.Phe1749Leu
XM_017000335.1:c.5241C>A	XP_016855824.1:p.Phe1747Leu
XM_017000337.1:c.3645C>A	XP_016855826.1:p.Phe1215Leu