Canonical Allele Identifier: CA341163598

Gene: COL11A1

Linked Data

• gnomAD v4: 1-102979073-T-C
• MyVariant Identifiers: chr1:g.103444629T>C (hg19) ; chr1:g.102979073T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979073T>C , CM000663.2:g.102979073T>C	GRCh38
NC_000001.10:g.103444629T>C , CM000663.1:g.103444629T>C	GRCh37
NC_000001.9:g.103217217T>C	NCBI36
NG_008033.1:g.134424A>G
NG_008033.2:g.134424A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2642A>G MANE Select	ENSP00000359114.3:p.Gln881Arg
ENST00000353414.8:c.2525A>G	ENSP00000302551.6:p.Gln842Arg
ENST00000358392.6:c.2678A>G	ENSP00000351163.2:p.Gln893Arg
ENST00000370096.7:c.2642A>G	ENSP00000359114.3:p.Gln881Arg
ENST00000512756.5:c.2294A>G	ENSP00000426533.1:p.Gln765Arg
ENST00000635193.1:c.1976A>G
NM_001190709.1:c.2525A>G	NP_001177638.1:p.Gln842Arg
NM_001854.3:c.2642A>G	NP_001845.3:p.Gln881Arg
NM_080629.2:c.2678A>G	NP_542196.2:p.Gln893Arg
NM_080630.3:c.2294A>G	NP_542197.3:p.Gln765Arg
XM_011540719.1:c.2642A>G	XP_011539021.1:p.Gln881Arg
XM_011540720.1:c.875A>G	XP_011539022.1:p.Gln292Arg
XM_011540721.1:c.230A>G	XP_011539023.1:p.Gln77Arg
XR_946545.1:n.3056A>G
NR_134980.1:n.2976A>G
XM_017000334.1:c.2795A>G	XP_016855823.1:p.Gln932Arg
XM_017000335.1:c.2789A>G	XP_016855824.1:p.Gln930Arg
XM_017000336.1:c.2795A>G	XP_016855825.1:p.Gln932Arg
XM_017000337.1:c.1193A>G	XP_016855826.1:p.Gln398Arg
NM_001854.4:c.2642A>G MANE Select	NP_001845.3:p.Gln881Arg
NM_080630.4:c.2294A>G	NP_542197.3:p.Gln765Arg
NR_134980.2:n.3002A>G
NM_001190709.2:c.2525A>G	NP_001177638.1:p.Gln842Arg
NM_080629.3:c.2678A>G	NP_542196.2:p.Gln893Arg