Canonical Allele Identifier: CA2574449711

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978771A>G , CM000663.2:g.102978771A>G	GRCh38
NC_000001.10:g.103444327A>G , CM000663.1:g.103444327A>G	GRCh37
NC_000001.9:g.103216915A>G	NCBI36
NG_008033.1:g.134726T>C
NG_008033.2:g.134726T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2710-19T>C MANE Select	ENSP00000359114.3:n.2710-19T>C
ENST00000353414.8:c.2593-19T>C	ENSP00000302551.6:n.2593-19T>C
ENST00000358392.6:c.2746-19T>C	ENSP00000351163.2:n.2746-19T>C
ENST00000370096.7:c.2710-19T>C	ENSP00000359114.3:n.2710-19T>C
ENST00000512756.5:c.2362-19T>C	ENSP00000426533.1:n.2362-19T>C
ENST00000635193.1:c.2044-19T>C
NM_001190709.1:c.2593-19T>C	NP_001177638.1:n.2593-19T>C
NM_001854.3:c.2710-19T>C	NP_001845.3:n.2710-19T>C
NM_080629.2:c.2746-19T>C	NP_542196.2:n.2746-19T>C
NM_080630.3:c.2362-19T>C	NP_542197.3:n.2362-19T>C
XM_011540719.1:c.2710-19T>C	XP_011539021.1:n.2710-19T>C
XM_011540720.1:c.943-19T>C	XP_011539022.1:n.943-19T>C
XM_011540721.1:c.298-19T>C	XP_011539023.1:n.298-19T>C
XR_946545.1:n.3124-19T>C
NR_134980.1:n.3044-19T>C
XM_017000334.1:c.2863-19T>C	XP_016855823.1:n.2863-19T>C
XM_017000335.1:c.2857-19T>C	XP_016855824.1:n.2857-19T>C
XM_017000336.1:c.2863-19T>C	XP_016855825.1:n.2863-19T>C
XM_017000337.1:c.1261-19T>C	XP_016855826.1:n.1261-19T>C
NM_001854.4:c.2710-19T>C MANE Select	NP_001845.3:n.2710-19T>C
NM_080630.4:c.2362-19T>C	NP_542197.3:n.2362-19T>C
NR_134980.2:n.3070-19T>C
NM_001190709.2:c.2593-19T>C	NP_001177638.1:n.2593-19T>C
NM_080629.3:c.2746-19T>C	NP_542196.2:n.2746-19T>C