Canonical Allele Identifier: CA341170822

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103412409G>T (hg19) ; chr1:g.102946853G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102946853G>T , CM000663.2:g.102946853G>T	GRCh38
NC_000001.10:g.103412409G>T , CM000663.1:g.103412409G>T	GRCh37
NC_000001.9:g.103184997G>T	NCBI36
NG_008033.1:g.166644C>A
NG_008033.2:g.166644C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3272C>A MANE Select	ENSP00000359114.3:p.Ala1091Asp
ENST00000353414.8:c.3155C>A	ENSP00000302551.6:p.Ala1052Asp
ENST00000358392.6:c.3308C>A	ENSP00000351163.2:p.Ala1103Asp
ENST00000370096.7:c.3272C>A	ENSP00000359114.3:p.Ala1091Asp
ENST00000512756.5:c.2924C>A	ENSP00000426533.1:p.Ala975Asp
ENST00000635193.1:c.2606C>A
NM_001190709.1:c.3155C>A	NP_001177638.1:p.Ala1052Asp
NM_001854.3:c.3272C>A	NP_001845.3:p.Ala1091Asp
NM_080629.2:c.3308C>A	NP_542196.2:p.Ala1103Asp
NM_080630.3:c.2924C>A	NP_542197.3:p.Ala975Asp
XM_011540719.1:c.3272C>A	XP_011539021.1:p.Ala1091Asp
XM_011540720.1:c.1505C>A	XP_011539022.1:p.Ala502Asp
XM_011540721.1:c.860C>A	XP_011539023.1:p.Ala287Asp
NR_134980.1:n.3606C>A
XM_017000334.1:c.3425C>A	XP_016855823.1:p.Ala1142Asp
XM_017000335.1:c.3419C>A	XP_016855824.1:p.Ala1140Asp
XM_017000336.1:c.3425C>A	XP_016855825.1:p.Ala1142Asp
XM_017000337.1:c.1823C>A	XP_016855826.1:p.Ala608Asp
NM_001854.4:c.3272C>A MANE Select	NP_001845.3:p.Ala1091Asp
NM_080630.4:c.2924C>A	NP_542197.3:p.Ala975Asp
NR_134980.2:n.3632C>A
NM_001190709.2:c.3155C>A	NP_001177638.1:p.Ala1052Asp
NM_080629.3:c.3308C>A	NP_542196.2:p.Ala1103Asp