Canonical Allele Identifier: CA341163288

Gene: COL11A1

Linked Data

• gnomAD v4: 1-102978886-C-T
• MyVariant Identifiers: chr1:g.103444442C>T (hg19) ; chr1:g.102978886C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978886C>T , CM000663.2:g.102978886C>T	GRCh38
NC_000001.10:g.103444442C>T , CM000663.1:g.103444442C>T	GRCh37
NC_000001.9:g.103217030C>T	NCBI36
NG_008033.1:g.134611G>A
NG_008033.2:g.134611G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2683G>A MANE Select	ENSP00000359114.3:p.Gly895Ser
ENST00000353414.8:c.2566G>A	ENSP00000302551.6:p.Gly856Ser
ENST00000358392.6:c.2719G>A	ENSP00000351163.2:p.Gly907Ser
ENST00000370096.7:c.2683G>A	ENSP00000359114.3:p.Gly895Ser
ENST00000512756.5:c.2335G>A	ENSP00000426533.1:p.Gly779Ser
ENST00000635193.1:c.2017G>A
NM_001190709.1:c.2566G>A	NP_001177638.1:p.Gly856Ser
NM_001854.3:c.2683G>A	NP_001845.3:p.Gly895Ser
NM_080629.2:c.2719G>A	NP_542196.2:p.Gly907Ser
NM_080630.3:c.2335G>A	NP_542197.3:p.Gly779Ser
XM_011540719.1:c.2683G>A	XP_011539021.1:p.Gly895Ser
XM_011540720.1:c.916G>A	XP_011539022.1:p.Gly306Ser
XM_011540721.1:c.271G>A	XP_011539023.1:p.Gly91Ser
XR_946545.1:n.3097G>A
NR_134980.1:n.3017G>A
XM_017000334.1:c.2836G>A	XP_016855823.1:p.Gly946Ser
XM_017000335.1:c.2830G>A	XP_016855824.1:p.Gly944Ser
XM_017000336.1:c.2836G>A	XP_016855825.1:p.Gly946Ser
XM_017000337.1:c.1234G>A	XP_016855826.1:p.Gly412Ser
NM_001854.4:c.2683G>A MANE Select	NP_001845.3:p.Gly895Ser
NM_080630.4:c.2335G>A	NP_542197.3:p.Gly779Ser
NR_134980.2:n.3043G>A
NM_001190709.2:c.2566G>A	NP_001177638.1:p.Gly856Ser
NM_080629.3:c.2719G>A	NP_542196.2:p.Gly907Ser