Canonical Allele Identifier: CA974712

Gene: COL11A1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.103003211A>T , CM000663.2:g.103003211A>T	GRCh38
NC_000001.10:g.103468767A>T , CM000663.1:g.103468767A>T	GRCh37
NC_000001.9:g.103241355A>T	NCBI36
NG_008033.1:g.110286T>A
NG_008033.2:g.110286T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.1998+4T>A MANE Select	ENSP00000359114.3:n.1998+4T>A
ENST00000461720.6:c.2151+4T>A	ENSP00000494909.1:n.2151+4T>A
ENST00000644186.1:c.1998+4T>A	ENSP00000493821.1:n.1998+4T>A
ENST00000645458.1:c.1998+4T>A	ENSP00000494179.1:n.1998+4T>A
ENST00000647280.1:c.1998+4T>A	ENSP00000494583.1:n.1998+4T>A
ENST00000353414.8:c.1881+4T>A	ENSP00000302551.6:n.1881+4T>A
ENST00000358392.6:c.2034+4T>A	ENSP00000351163.2:n.2034+4T>A
ENST00000370096.7:c.1998+4T>A	ENSP00000359114.3:n.1998+4T>A
ENST00000461720.5:n.346+4T>A
ENST00000475980.1:n.39-420T>A
ENST00000512756.5:c.1650+4T>A	ENSP00000426533.1:n.1650+4T>A
ENST00000635193.1:c.1316+4T>A
NM_001190709.1:c.1881+4T>A	NP_001177638.1:n.1881+4T>A
NM_001854.3:c.1998+4T>A	NP_001845.3:n.1998+4T>A
NM_080629.2:c.2034+4T>A	NP_542196.2:n.2034+4T>A
NM_080630.3:c.1650+4T>A	NP_542197.3:n.1650+4T>A
XM_011540719.1:c.1998+4T>A	XP_011539021.1:n.1998+4T>A
XM_011540720.1:c.231+4T>A	XP_011539022.1:n.231+4T>A
XM_011540721.1:c.-431+4T>A	XP_011539023.1:n.-431+4T>A
XR_946545.1:n.2396+4T>A
NR_134980.1:n.2316+4T>A
XM_017000334.1:c.2151+4T>A	XP_016855823.1:n.2151+4T>A
XM_017000335.1:c.2145+4T>A	XP_016855824.1:n.2145+4T>A
XM_017000336.1:c.2151+4T>A	XP_016855825.1:n.2151+4T>A
XM_017000337.1:c.549+4T>A	XP_016855826.1:n.549+4T>A
NM_001854.4:c.1998+4T>A MANE Select	NP_001845.3:n.1998+4T>A
NM_080630.4:c.1650+4T>A	NP_542197.3:n.1650+4T>A
NR_134980.2:n.2342+4T>A
NM_001190709.2:c.1881+4T>A	NP_001177638.1:n.1881+4T>A
NM_080629.3:c.2034+4T>A	NP_542196.2:n.2034+4T>A