Canonical Allele Identifier: CA341163790

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444659C>A (hg19) ; chr1:g.102979103C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102979103C>A , CM000663.2:g.102979103C>A	GRCh38
NC_000001.10:g.103444659C>A , CM000663.1:g.103444659C>A	GRCh37
NC_000001.9:g.103217247C>A	NCBI36
NG_008033.1:g.134394G>T
NG_008033.2:g.134394G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2612G>T MANE Select	ENSP00000359114.3:p.Gly871Val
ENST00000353414.8:c.2495G>T	ENSP00000302551.6:p.Gly832Val
ENST00000358392.6:c.2648G>T	ENSP00000351163.2:p.Gly883Val
ENST00000370096.7:c.2612G>T	ENSP00000359114.3:p.Gly871Val
ENST00000512756.5:c.2264G>T	ENSP00000426533.1:p.Gly755Val
ENST00000635193.1:c.1946G>T
NM_001190709.1:c.2495G>T	NP_001177638.1:p.Gly832Val
NM_001854.3:c.2612G>T	NP_001845.3:p.Gly871Val
NM_080629.2:c.2648G>T	NP_542196.2:p.Gly883Val
NM_080630.3:c.2264G>T	NP_542197.3:p.Gly755Val
XM_011540719.1:c.2612G>T	XP_011539021.1:p.Gly871Val
XM_011540720.1:c.845G>T	XP_011539022.1:p.Gly282Val
XM_011540721.1:c.200G>T	XP_011539023.1:p.Gly67Val
XR_946545.1:n.3026G>T
NR_134980.1:n.2946G>T
XM_017000334.1:c.2765G>T	XP_016855823.1:p.Gly922Val
XM_017000335.1:c.2759G>T	XP_016855824.1:p.Gly920Val
XM_017000336.1:c.2765G>T	XP_016855825.1:p.Gly922Val
XM_017000337.1:c.1163G>T	XP_016855826.1:p.Gly388Val
NM_001854.4:c.2612G>T MANE Select	NP_001845.3:p.Gly871Val
NM_080630.4:c.2264G>T	NP_542197.3:p.Gly755Val
NR_134980.2:n.2972G>T
NM_001190709.2:c.2495G>T	NP_001177638.1:p.Gly832Val
NM_080629.3:c.2648G>T	NP_542196.2:p.Gly883Val