Canonical Allele Identifier: CA341163621

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444632C>T (hg19) ; chr1:g.102979076C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979076C>T , CM000663.2:g.102979076C>T	GRCh38
NC_000001.10:g.103444632C>T , CM000663.1:g.103444632C>T	GRCh37
NC_000001.9:g.103217220C>T	NCBI36
NG_008033.1:g.134421G>A
NG_008033.2:g.134421G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2639G>A MANE Select	ENSP00000359114.3:p.Gly880Asp
ENST00000353414.8:c.2522G>A	ENSP00000302551.6:p.Gly841Asp
ENST00000358392.6:c.2675G>A	ENSP00000351163.2:p.Gly892Asp
ENST00000370096.7:c.2639G>A	ENSP00000359114.3:p.Gly880Asp
ENST00000512756.5:c.2291G>A	ENSP00000426533.1:p.Gly764Asp
ENST00000635193.1:c.1973G>A
NM_001190709.1:c.2522G>A	NP_001177638.1:p.Gly841Asp
NM_001854.3:c.2639G>A	NP_001845.3:p.Gly880Asp
NM_080629.2:c.2675G>A	NP_542196.2:p.Gly892Asp
NM_080630.3:c.2291G>A	NP_542197.3:p.Gly764Asp
XM_011540719.1:c.2639G>A	XP_011539021.1:p.Gly880Asp
XM_011540720.1:c.872G>A	XP_011539022.1:p.Gly291Asp
XM_011540721.1:c.227G>A	XP_011539023.1:p.Gly76Asp
XR_946545.1:n.3053G>A
NR_134980.1:n.2973G>A
XM_017000334.1:c.2792G>A	XP_016855823.1:p.Gly931Asp
XM_017000335.1:c.2786G>A	XP_016855824.1:p.Gly929Asp
XM_017000336.1:c.2792G>A	XP_016855825.1:p.Gly931Asp
XM_017000337.1:c.1190G>A	XP_016855826.1:p.Gly397Asp
NM_001854.4:c.2639G>A MANE Select	NP_001845.3:p.Gly880Asp
NM_080630.4:c.2291G>A	NP_542197.3:p.Gly764Asp
NR_134980.2:n.2999G>A
NM_001190709.2:c.2522G>A	NP_001177638.1:p.Gly841Asp
NM_080629.3:c.2675G>A	NP_542196.2:p.Gly892Asp