Canonical Allele Identifier: CA341162962

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444292T>A (hg19) ; chr1:g.102978736T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978736T>A , CM000663.2:g.102978736T>A	GRCh38
NC_000001.10:g.103444292T>A , CM000663.1:g.103444292T>A	GRCh37
NC_000001.9:g.103216880T>A	NCBI36
NG_008033.1:g.134761A>T
NG_008033.2:g.134761A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2726A>T MANE Select	ENSP00000359114.3:p.Asp909Val
ENST00000353414.8:c.2609A>T	ENSP00000302551.6:p.Asp870Val
ENST00000358392.6:c.2762A>T	ENSP00000351163.2:p.Asp921Val
ENST00000370096.7:c.2726A>T	ENSP00000359114.3:p.Asp909Val
ENST00000512756.5:c.2378A>T	ENSP00000426533.1:p.Asp793Val
ENST00000635193.1:c.2060A>T
NM_001190709.1:c.2609A>T	NP_001177638.1:p.Asp870Val
NM_001854.3:c.2726A>T	NP_001845.3:p.Asp909Val
NM_080629.2:c.2762A>T	NP_542196.2:p.Asp921Val
NM_080630.3:c.2378A>T	NP_542197.3:p.Asp793Val
XM_011540719.1:c.2726A>T	XP_011539021.1:p.Asp909Val
XM_011540720.1:c.959A>T	XP_011539022.1:p.Asp320Val
XM_011540721.1:c.314A>T	XP_011539023.1:p.Asp105Val
XR_946545.1:n.3140A>T
NR_134980.1:n.3060A>T
XM_017000334.1:c.2879A>T	XP_016855823.1:p.Asp960Val
XM_017000335.1:c.2873A>T	XP_016855824.1:p.Asp958Val
XM_017000336.1:c.2879A>T	XP_016855825.1:p.Asp960Val
XM_017000337.1:c.1277A>T	XP_016855826.1:p.Asp426Val
NM_001854.4:c.2726A>T MANE Select	NP_001845.3:p.Asp909Val
NM_080630.4:c.2378A>T	NP_542197.3:p.Asp793Val
NR_134980.2:n.3086A>T
NM_001190709.2:c.2609A>T	NP_001177638.1:p.Asp870Val
NM_080629.3:c.2762A>T	NP_542196.2:p.Asp921Val