Canonical Allele Identifier: CA1185276613

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102989543C= , CM000663.2:g.102989543C=	GRCh38
NC_000001.10:g.103455099C= , CM000663.1:g.103455099C=	GRCh37
NC_000001.9:g.103227687C=	NCBI36
NG_008033.1:g.123954G=
NG_008033.2:g.123954G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2369G= MANE Select	ENSP00000359114.3:p.Gly790=
ENST00000353414.8:c.2252G=	ENSP00000302551.6:p.Gly751=
ENST00000358392.6:c.2405G=	ENSP00000351163.2:p.Gly802=
ENST00000370096.7:c.2369G=	ENSP00000359114.3:p.Gly790=
ENST00000512756.5:c.2021G=	ENSP00000426533.1:p.Gly674=
ENST00000635193.1:c.1687G=
NM_001190709.1:c.2252G=	NP_001177638.1:p.Gly751=
NM_001854.3:c.2369G=	NP_001845.3:p.Gly790=
NM_080629.2:c.2405G=	NP_542196.2:p.Gly802=
NM_080630.3:c.2021G=	NP_542197.3:p.Gly674=
XM_011540719.1:c.2369G=	XP_011539021.1:p.Gly790=
XM_011540720.1:c.602G=	XP_011539022.1:p.Gly201=
XM_011540721.1:c.-60G=	XP_011539023.1:n.-60G=
XR_946545.1:n.2767G=
NR_134980.1:n.2687G=
XM_017000334.1:c.2522G=	XP_016855823.1:p.Gly841=
XM_017000335.1:c.2516G=	XP_016855824.1:p.Gly839=
XM_017000336.1:c.2522G=	XP_016855825.1:p.Gly841=
XM_017000337.1:c.920G=	XP_016855826.1:p.Gly307=
NM_001854.4:c.2369G= MANE Select	NP_001845.3:p.Gly790=
NM_080630.4:c.2021G=	NP_542197.3:p.Gly674=
NR_134980.2:n.2713G=
NM_001190709.2:c.2252G=	NP_001177638.1:p.Gly751=
NM_080629.3:c.2405G=	NP_542196.2:p.Gly802=