Canonical Allele Identifier: CA27703169

Gene: COL11A1

Linked Data

• dbSNP Id: rs1011778181
• gnomAD v2: 1-103444366-T-C
• gnomAD v3: 1-102978810-T-C
• gnomAD v4: 1-102978810-T-C
• MyVariant Identifiers: chr1:g.103444366T>C (hg19) ; chr1:g.102978810T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978810T>C , CM000663.2:g.102978810T>C	GRCh38
NC_000001.10:g.103444366T>C , CM000663.1:g.103444366T>C	GRCh37
NC_000001.9:g.103216954T>C	NCBI36
NG_008033.1:g.134687A>G
NG_008033.2:g.134687A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2709+50A>G MANE Select	ENSP00000359114.3:n.2709+50A>G
ENST00000353414.8:c.2592+50A>G	ENSP00000302551.6:n.2592+50A>G
ENST00000358392.6:c.2745+50A>G	ENSP00000351163.2:n.2745+50A>G
ENST00000370096.7:c.2709+50A>G	ENSP00000359114.3:n.2709+50A>G
ENST00000512756.5:c.2361+50A>G	ENSP00000426533.1:n.2361+50A>G
ENST00000635193.1:c.2043+50A>G
NM_001190709.1:c.2592+50A>G	NP_001177638.1:n.2592+50A>G
NM_001854.3:c.2709+50A>G	NP_001845.3:n.2709+50A>G
NM_080629.2:c.2745+50A>G	NP_542196.2:n.2745+50A>G
NM_080630.3:c.2361+50A>G	NP_542197.3:n.2361+50A>G
XM_011540719.1:c.2709+50A>G	XP_011539021.1:n.2709+50A>G
XM_011540720.1:c.942+50A>G	XP_011539022.1:n.942+50A>G
XM_011540721.1:c.297+50A>G	XP_011539023.1:n.297+50A>G
XR_946545.1:n.3123+50A>G
NR_134980.1:n.3043+50A>G
XM_017000334.1:c.2862+50A>G	XP_016855823.1:n.2862+50A>G
XM_017000335.1:c.2856+50A>G	XP_016855824.1:n.2856+50A>G
XM_017000336.1:c.2862+50A>G	XP_016855825.1:n.2862+50A>G
XM_017000337.1:c.1260+50A>G	XP_016855826.1:n.1260+50A>G
NM_001854.4:c.2709+50A>G MANE Select	NP_001845.3:n.2709+50A>G
NM_080630.4:c.2361+50A>G	NP_542197.3:n.2361+50A>G
NR_134980.2:n.3069+50A>G
NM_001190709.2:c.2592+50A>G	NP_001177638.1:n.2592+50A>G
NM_080629.3:c.2745+50A>G	NP_542196.2:n.2745+50A>G