Canonical Allele Identifier: CA341163095

Gene: COL11A1

Linked Data

• MyVariant Identifiers: chr1:g.103444307C>T (hg19) ; chr1:g.102978751C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978751C>T , CM000663.2:g.102978751C>T	GRCh38
NC_000001.10:g.103444307C>T , CM000663.1:g.103444307C>T	GRCh37
NC_000001.9:g.103216895C>T	NCBI36
NG_008033.1:g.134746G>A
NG_008033.2:g.134746G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2711G>A MANE Select	ENSP00000359114.3:p.Gly904Asp
ENST00000353414.8:c.2594G>A	ENSP00000302551.6:p.Gly865Asp
ENST00000358392.6:c.2747G>A	ENSP00000351163.2:p.Gly916Asp
ENST00000370096.7:c.2711G>A	ENSP00000359114.3:p.Gly904Asp
ENST00000512756.5:c.2363G>A	ENSP00000426533.1:p.Gly788Asp
ENST00000635193.1:c.2045G>A
NM_001190709.1:c.2594G>A	NP_001177638.1:p.Gly865Asp
NM_001854.3:c.2711G>A	NP_001845.3:p.Gly904Asp
NM_080629.2:c.2747G>A	NP_542196.2:p.Gly916Asp
NM_080630.3:c.2363G>A	NP_542197.3:p.Gly788Asp
XM_011540719.1:c.2711G>A	XP_011539021.1:p.Gly904Asp
XM_011540720.1:c.944G>A	XP_011539022.1:p.Gly315Asp
XM_011540721.1:c.299G>A	XP_011539023.1:p.Gly100Asp
XR_946545.1:n.3125G>A
NR_134980.1:n.3045G>A
XM_017000334.1:c.2864G>A	XP_016855823.1:p.Gly955Asp
XM_017000335.1:c.2858G>A	XP_016855824.1:p.Gly953Asp
XM_017000336.1:c.2864G>A	XP_016855825.1:p.Gly955Asp
XM_017000337.1:c.1262G>A	XP_016855826.1:p.Gly421Asp
NM_001854.4:c.2711G>A MANE Select	NP_001845.3:p.Gly904Asp
NM_080630.4:c.2363G>A	NP_542197.3:p.Gly788Asp
NR_134980.2:n.3071G>A
NM_001190709.2:c.2594G>A	NP_001177638.1:p.Gly865Asp
NM_080629.3:c.2747G>A	NP_542196.2:p.Gly916Asp