Canonical Allele Identifier: CA341163071

Gene: COL11A1

Linked Data

• COSMIC: COSM4412133 ; COSM4412134
• MyVariant Identifiers: chr1:g.103444304G>T (hg19) ; chr1:g.102978748G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978748G>T , CM000663.2:g.102978748G>T	GRCh38
NC_000001.10:g.103444304G>T , CM000663.1:g.103444304G>T	GRCh37
NC_000001.9:g.103216892G>T	NCBI36
NG_008033.1:g.134749C>A
NG_008033.2:g.134749C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2714C>A MANE Select	ENSP00000359114.3:p.Thr905Asn
ENST00000353414.8:c.2597C>A	ENSP00000302551.6:p.Thr866Asn
ENST00000358392.6:c.2750C>A	ENSP00000351163.2:p.Thr917Asn
ENST00000370096.7:c.2714C>A	ENSP00000359114.3:p.Thr905Asn
ENST00000512756.5:c.2366C>A	ENSP00000426533.1:p.Thr789Asn
ENST00000635193.1:c.2048C>A
NM_001190709.1:c.2597C>A	NP_001177638.1:p.Thr866Asn
NM_001854.3:c.2714C>A	NP_001845.3:p.Thr905Asn
NM_080629.2:c.2750C>A	NP_542196.2:p.Thr917Asn
NM_080630.3:c.2366C>A	NP_542197.3:p.Thr789Asn
XM_011540719.1:c.2714C>A	XP_011539021.1:p.Thr905Asn
XM_011540720.1:c.947C>A	XP_011539022.1:p.Thr316Asn
XM_011540721.1:c.302C>A	XP_011539023.1:p.Thr101Asn
XR_946545.1:n.3128C>A
NR_134980.1:n.3048C>A
XM_017000334.1:c.2867C>A	XP_016855823.1:p.Thr956Asn
XM_017000335.1:c.2861C>A	XP_016855824.1:p.Thr954Asn
XM_017000336.1:c.2867C>A	XP_016855825.1:p.Thr956Asn
XM_017000337.1:c.1265C>A	XP_016855826.1:p.Thr422Asn
NM_001854.4:c.2714C>A MANE Select	NP_001845.3:p.Thr905Asn
NM_080630.4:c.2366C>A	NP_542197.3:p.Thr789Asn
NR_134980.2:n.3074C>A
NM_001190709.2:c.2597C>A	NP_001177638.1:p.Thr866Asn
NM_080629.3:c.2750C>A	NP_542196.2:p.Thr917Asn