Canonical Allele Identifier: CA341162272

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102974885T>C , CM000663.2:g.102974885T>C	GRCh38
NC_000001.10:g.103440441T>C , CM000663.1:g.103440441T>C	GRCh37
NC_000001.9:g.103213029T>C	NCBI36
NG_008033.1:g.138612A>G
NG_008033.2:g.138612A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001854.4:c.2755-2A>G MANE Select	NP_001845.3:n.2755-2A>G
ENST00000370096.9:c.2755-2A>G MANE Select	ENSP00000359114.3:n.2755-2A>G
NM_001190709.1:c.2638-2A>G	NP_001177638.1:n.2638-2A>G
NM_001190709.2:c.2638-2A>G	NP_001177638.1:n.2638-2A>G
NM_001854.3:c.2755-2A>G	NP_001845.3:n.2755-2A>G
NM_080629.2:c.2791-2A>G	NP_542196.2:n.2791-2A>G
NM_080629.3:c.2791-2A>G	NP_542196.2:n.2791-2A>G
NM_080630.3:c.2407-2A>G	NP_542197.3:n.2407-2A>G
NM_080630.4:c.2407-2A>G	NP_542197.3:n.2407-2A>G
NR_134980.1:n.3089-2A>G
NR_134980.2:n.3115-2A>G
ENST00000353414.8:c.2638-2A>G	ENSP00000302551.6:n.2638-2A>G
ENST00000358392.6:c.2791-2A>G	ENSP00000351163.2:n.2791-2A>G
ENST00000370096.7:c.2755-2A>G	ENSP00000359114.3:n.2755-2A>G
ENST00000512756.5:c.2407-2A>G	ENSP00000426533.1:n.2407-2A>G
ENST00000635193.1:c.2089-2A>G
XM_011540719.1:c.2755-2A>G	XP_011539021.1:n.2755-2A>G
XM_011540720.1:c.988-2A>G	XP_011539022.1:n.988-2A>G
XM_011540721.1:c.343-2A>G	XP_011539023.1:n.343-2A>G
XM_017000334.1:c.2908-2A>G	XP_016855823.1:n.2908-2A>G
XM_017000335.1:c.2902-2A>G	XP_016855824.1:n.2902-2A>G
XM_017000336.1:c.2908-2A>G	XP_016855825.1:n.2908-2A>G
XM_017000337.1:c.1306-2A>G	XP_016855826.1:n.1306-2A>G
XR_946545.1:n.3169-2A>G