Canonical Allele Identifier: CA341162910

Gene: COL11A1

Linked Data

• ClinVar Variation Id: 1485804
• ClinVar RCV Id: RCV002001007
• dbSNP Id: rs2101678875
• MyVariant Identifiers: chr1:g.103444277G>A (hg19) ; chr1:g.102978721G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978721G>A , CM000663.2:g.102978721G>A	GRCh38
NC_000001.10:g.103444277G>A , CM000663.1:g.103444277G>A	GRCh37
NC_000001.9:g.103216865G>A	NCBI36
NG_008033.1:g.134776C>T
NG_008033.2:g.134776C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2741C>T MANE Select	ENSP00000359114.3:p.Pro914Leu
ENST00000353414.8:c.2624C>T	ENSP00000302551.6:p.Pro875Leu
ENST00000358392.6:c.2777C>T	ENSP00000351163.2:p.Pro926Leu
ENST00000370096.7:c.2741C>T	ENSP00000359114.3:p.Pro914Leu
ENST00000512756.5:c.2393C>T	ENSP00000426533.1:p.Pro798Leu
ENST00000635193.1:c.2075C>T
NM_001190709.1:c.2624C>T	NP_001177638.1:p.Pro875Leu
NM_001854.3:c.2741C>T	NP_001845.3:p.Pro914Leu
NM_080629.2:c.2777C>T	NP_542196.2:p.Pro926Leu
NM_080630.3:c.2393C>T	NP_542197.3:p.Pro798Leu
XM_011540719.1:c.2741C>T	XP_011539021.1:p.Pro914Leu
XM_011540720.1:c.974C>T	XP_011539022.1:p.Pro325Leu
XM_011540721.1:c.329C>T	XP_011539023.1:p.Pro110Leu
XR_946545.1:n.3155C>T
NR_134980.1:n.3075C>T
XM_017000334.1:c.2894C>T	XP_016855823.1:p.Pro965Leu
XM_017000335.1:c.2888C>T	XP_016855824.1:p.Pro963Leu
XM_017000336.1:c.2894C>T	XP_016855825.1:p.Pro965Leu
XM_017000337.1:c.1292C>T	XP_016855826.1:p.Pro431Leu
NM_001854.4:c.2741C>T MANE Select	NP_001845.3:p.Pro914Leu
NM_080630.4:c.2393C>T	NP_542197.3:p.Pro798Leu
NR_134980.2:n.3101C>T
NM_001190709.2:c.2624C>T	NP_001177638.1:p.Pro875Leu
NM_080629.3:c.2777C>T	NP_542196.2:p.Pro926Leu