Canonical Allele Identifier: CA341162955

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444290C>G (hg19) ; chr1:g.102978734C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978734C>G , CM000663.2:g.102978734C>G	GRCh38
NC_000001.10:g.103444290C>G , CM000663.1:g.103444290C>G	GRCh37
NC_000001.9:g.103216878C>G	NCBI36
NG_008033.1:g.134763G>C
NG_008033.2:g.134763G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2728G>C MANE Select	ENSP00000359114.3:p.Gly910Arg
ENST00000353414.8:c.2611G>C	ENSP00000302551.6:p.Gly871Arg
ENST00000358392.6:c.2764G>C	ENSP00000351163.2:p.Gly922Arg
ENST00000370096.7:c.2728G>C	ENSP00000359114.3:p.Gly910Arg
ENST00000512756.5:c.2380G>C	ENSP00000426533.1:p.Gly794Arg
ENST00000635193.1:c.2062G>C
NM_001190709.1:c.2611G>C	NP_001177638.1:p.Gly871Arg
NM_001854.3:c.2728G>C	NP_001845.3:p.Gly910Arg
NM_080629.2:c.2764G>C	NP_542196.2:p.Gly922Arg
NM_080630.3:c.2380G>C	NP_542197.3:p.Gly794Arg
XM_011540719.1:c.2728G>C	XP_011539021.1:p.Gly910Arg
XM_011540720.1:c.961G>C	XP_011539022.1:p.Gly321Arg
XM_011540721.1:c.316G>C	XP_011539023.1:p.Gly106Arg
XR_946545.1:n.3142G>C
NR_134980.1:n.3062G>C
XM_017000334.1:c.2881G>C	XP_016855823.1:p.Gly961Arg
XM_017000335.1:c.2875G>C	XP_016855824.1:p.Gly959Arg
XM_017000336.1:c.2881G>C	XP_016855825.1:p.Gly961Arg
XM_017000337.1:c.1279G>C	XP_016855826.1:p.Gly427Arg
NM_001854.4:c.2728G>C MANE Select	NP_001845.3:p.Gly910Arg
NM_080630.4:c.2380G>C	NP_542197.3:p.Gly794Arg
NR_134980.2:n.3088G>C
NM_001190709.2:c.2611G>C	NP_001177638.1:p.Gly871Arg
NM_080629.3:c.2764G>C	NP_542196.2:p.Gly922Arg