Canonical Allele Identifier: CA341171424

Gene: COL11A1

Linked Data

• gnomAD v4: 1-102946941-G-T
• MyVariant Identifiers: chr1:g.103412497G>T (hg19) ; chr1:g.102946941G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102946941G>T , CM000663.2:g.102946941G>T	GRCh38
NC_000001.10:g.103412497G>T , CM000663.1:g.103412497G>T	GRCh37
NC_000001.9:g.103185085G>T	NCBI36
NG_008033.1:g.166556C>A
NG_008033.2:g.166556C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3184C>A MANE Select	ENSP00000359114.3:p.Arg1062Ser
ENST00000353414.8:c.3067C>A	ENSP00000302551.6:p.Arg1023Ser
ENST00000358392.6:c.3220C>A	ENSP00000351163.2:p.Arg1074Ser
ENST00000370096.7:c.3184C>A	ENSP00000359114.3:p.Arg1062Ser
ENST00000512756.5:c.2836C>A	ENSP00000426533.1:p.Arg946Ser
ENST00000635193.1:c.2518C>A
NM_001190709.1:c.3067C>A	NP_001177638.1:p.Arg1023Ser
NM_001854.3:c.3184C>A	NP_001845.3:p.Arg1062Ser
NM_080629.2:c.3220C>A	NP_542196.2:p.Arg1074Ser
NM_080630.3:c.2836C>A	NP_542197.3:p.Arg946Ser
XM_011540719.1:c.3184C>A	XP_011539021.1:p.Arg1062Ser
XM_011540720.1:c.1417C>A	XP_011539022.1:p.Arg473Ser
XM_011540721.1:c.772C>A	XP_011539023.1:p.Arg258Ser
NR_134980.1:n.3518C>A
XM_017000334.1:c.3337C>A	XP_016855823.1:p.Arg1113Ser
XM_017000335.1:c.3331C>A	XP_016855824.1:p.Arg1111Ser
XM_017000336.1:c.3337C>A	XP_016855825.1:p.Arg1113Ser
XM_017000337.1:c.1735C>A	XP_016855826.1:p.Arg579Ser
NM_001854.4:c.3184C>A MANE Select	NP_001845.3:p.Arg1062Ser
NM_080630.4:c.2836C>A	NP_542197.3:p.Arg946Ser
NR_134980.2:n.3544C>A
NM_001190709.2:c.3067C>A	NP_001177638.1:p.Arg1023Ser
NM_080629.3:c.3220C>A	NP_542196.2:p.Arg1074Ser