Canonical Allele Identifier: CA2744832736

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102993855A>T , CM000663.2:g.102993855A>T	GRCh38
NC_000001.10:g.103459411A>T , CM000663.1:g.103459411A>T	GRCh37
NC_000001.9:g.103231999A>T	NCBI36
NG_008033.1:g.119642T>A
NG_008033.2:g.119642T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2340+2009T>A MANE Select	ENSP00000359114.3:n.2340+2009T>A
ENST00000353414.8:c.2223+2009T>A	ENSP00000302551.6:n.2223+2009T>A
ENST00000358392.6:c.2376+2009T>A	ENSP00000351163.2:n.2376+2009T>A
ENST00000370096.7:c.2340+2009T>A	ENSP00000359114.3:n.2340+2009T>A
ENST00000512756.5:c.1992+2009T>A	ENSP00000426533.1:n.1992+2009T>A
ENST00000635193.1:c.1658+2009T>A
NM_001190709.1:c.2223+2009T>A	NP_001177638.1:n.2223+2009T>A
NM_001854.3:c.2340+2009T>A	NP_001845.3:n.2340+2009T>A
NM_080629.2:c.2376+2009T>A	NP_542196.2:n.2376+2009T>A
NM_080630.3:c.1992+2009T>A	NP_542197.3:n.1992+2009T>A
XM_011540719.1:c.2340+2009T>A	XP_011539021.1:n.2340+2009T>A
XM_011540720.1:c.573+2009T>A	XP_011539022.1:n.573+2009T>A
XM_011540721.1:c.-89+2009T>A	XP_011539023.1:n.-89+2009T>A
XR_946545.1:n.2738+2009T>A
NR_134980.1:n.2658+2009T>A
XM_017000334.1:c.2493+2009T>A	XP_016855823.1:n.2493+2009T>A
XM_017000335.1:c.2487+2009T>A	XP_016855824.1:n.2487+2009T>A
XM_017000336.1:c.2493+2009T>A	XP_016855825.1:n.2493+2009T>A
XM_017000337.1:c.891+2009T>A	XP_016855826.1:n.891+2009T>A
NM_001854.4:c.2340+2009T>A MANE Select	NP_001845.3:n.2340+2009T>A
NM_080630.4:c.1992+2009T>A	NP_542197.3:n.1992+2009T>A
NR_134980.2:n.2684+2009T>A
NM_001190709.2:c.2223+2009T>A	NP_001177638.1:n.2223+2009T>A
NM_080629.3:c.2376+2009T>A	NP_542196.2:n.2376+2009T>A