Canonical Allele Identifier: CA973679

Gene: COL11A1

Linked Data

• dbSNP Id: rs748324856
• ExAC: 1:103364573 A / G
• gnomAD v2: 1-103364573-A-G
• gnomAD v3: 1-102899017-A-G
• gnomAD v4: 1-102899017-A-G
• MyVariant Identifiers: chr1:g.103364573A>G (hg19) ; chr1:g.102899017A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102899017A>G , CM000663.2:g.102899017A>G	GRCh38
NC_000001.10:g.103364573A>G , CM000663.1:g.103364573A>G	GRCh37
NC_000001.9:g.103137161A>G	NCBI36
NG_008033.1:g.214480T>C
NG_008033.2:g.214480T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370096.9:c.4087-23T>C MANE Select	ENSP00000359114.3:n.4087-23T>C
ENST00000353414.8:c.3970-23T>C	ENSP00000302551.6:n.3970-23T>C
ENST00000358392.6:c.4123-23T>C	ENSP00000351163.2:n.4123-23T>C
ENST00000370096.7:c.4087-23T>C	ENSP00000359114.3:n.4087-23T>C
ENST00000512756.5:c.3739-23T>C	ENSP00000426533.1:n.3739-23T>C
ENST00000635193.1:c.3421-23T>C
NM_001190709.1:c.3970-23T>C	NP_001177638.1:n.3970-23T>C
NM_001854.3:c.4087-23T>C	NP_001845.3:n.4087-23T>C
NM_080629.2:c.4123-23T>C	NP_542196.2:n.4123-23T>C
NM_080630.3:c.3739-23T>C	NP_542197.3:n.3739-23T>C
XM_011540719.1:c.4087-23T>C	XP_011539021.1:n.4087-23T>C
XM_011540720.1:c.2320-23T>C	XP_011539022.1:n.2320-23T>C
XM_011540721.1:c.1675-23T>C	XP_011539023.1:n.1675-23T>C
NR_134980.1:n.4421-23T>C
XM_017000334.1:c.4240-23T>C	XP_016855823.1:n.4240-23T>C
XM_017000335.1:c.4234-23T>C	XP_016855824.1:n.4234-23T>C
XM_017000336.1:c.4240-23T>C	XP_016855825.1:n.4240-23T>C
XM_017000337.1:c.2638-23T>C	XP_016855826.1:n.2638-23T>C
NM_001854.4:c.4087-23T>C MANE Select	NP_001845.3:n.4087-23T>C
NM_080630.4:c.3739-23T>C	NP_542197.3:n.3739-23T>C
NR_134980.2:n.4447-23T>C
NM_001190709.2:c.3970-23T>C	NP_001177638.1:n.3970-23T>C
NM_080629.3:c.4123-23T>C	NP_542196.2:n.4123-23T>C