Canonical Allele Identifier: CA341163695

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444645G>T (hg19) ; chr1:g.102979089G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979089G>T , CM000663.2:g.102979089G>T	GRCh38
NC_000001.10:g.103444645G>T , CM000663.1:g.103444645G>T	GRCh37
NC_000001.9:g.103217233G>T	NCBI36
NG_008033.1:g.134408C>A
NG_008033.2:g.134408C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2626C>A MANE Select	ENSP00000359114.3:p.Pro876Thr
ENST00000353414.8:c.2509C>A	ENSP00000302551.6:p.Pro837Thr
ENST00000358392.6:c.2662C>A	ENSP00000351163.2:p.Pro888Thr
ENST00000370096.7:c.2626C>A	ENSP00000359114.3:p.Pro876Thr
ENST00000512756.5:c.2278C>A	ENSP00000426533.1:p.Pro760Thr
ENST00000635193.1:c.1960C>A
NM_001190709.1:c.2509C>A	NP_001177638.1:p.Pro837Thr
NM_001854.3:c.2626C>A	NP_001845.3:p.Pro876Thr
NM_080629.2:c.2662C>A	NP_542196.2:p.Pro888Thr
NM_080630.3:c.2278C>A	NP_542197.3:p.Pro760Thr
XM_011540719.1:c.2626C>A	XP_011539021.1:p.Pro876Thr
XM_011540720.1:c.859C>A	XP_011539022.1:p.Pro287Thr
XM_011540721.1:c.214C>A	XP_011539023.1:p.Pro72Thr
XR_946545.1:n.3040C>A
NR_134980.1:n.2960C>A
XM_017000334.1:c.2779C>A	XP_016855823.1:p.Pro927Thr
XM_017000335.1:c.2773C>A	XP_016855824.1:p.Pro925Thr
XM_017000336.1:c.2779C>A	XP_016855825.1:p.Pro927Thr
XM_017000337.1:c.1177C>A	XP_016855826.1:p.Pro393Thr
NM_001854.4:c.2626C>A MANE Select	NP_001845.3:p.Pro876Thr
NM_080630.4:c.2278C>A	NP_542197.3:p.Pro760Thr
NR_134980.2:n.2986C>A
NM_001190709.2:c.2509C>A	NP_001177638.1:p.Pro837Thr
NM_080629.3:c.2662C>A	NP_542196.2:p.Pro888Thr