Canonical Allele Identifier: CA1185271974

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102978865G= , CM000663.2:g.102978865G=	GRCh38
NC_000001.10:g.103444421G= , CM000663.1:g.103444421G=	GRCh37
NC_000001.9:g.103217009G=	NCBI36
NG_008033.1:g.134632C=
NG_008033.2:g.134632C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2704C= MANE Select	ENSP00000359114.3:p.Pro902=
ENST00000353414.8:c.2587C=	ENSP00000302551.6:p.Pro863=
ENST00000358392.6:c.2740C=	ENSP00000351163.2:p.Pro914=
ENST00000370096.7:c.2704C=	ENSP00000359114.3:p.Pro902=
ENST00000512756.5:c.2356C=	ENSP00000426533.1:p.Pro786=
ENST00000635193.1:c.2038C=
NM_001190709.1:c.2587C=	NP_001177638.1:p.Pro863=
NM_001854.3:c.2704C=	NP_001845.3:p.Pro902=
NM_080629.2:c.2740C=	NP_542196.2:p.Pro914=
NM_080630.3:c.2356C=	NP_542197.3:p.Pro786=
XM_011540719.1:c.2704C=	XP_011539021.1:p.Pro902=
XM_011540720.1:c.937C=	XP_011539022.1:p.Pro313=
XM_011540721.1:c.292C=	XP_011539023.1:p.Pro98=
XR_946545.1:n.3118C=
NR_134980.1:n.3038C=
XM_017000334.1:c.2857C=	XP_016855823.1:p.Pro953=
XM_017000335.1:c.2851C=	XP_016855824.1:p.Pro951=
XM_017000336.1:c.2857C=	XP_016855825.1:p.Pro953=
XM_017000337.1:c.1255C=	XP_016855826.1:p.Pro419=
NM_001854.4:c.2704C= MANE Select	NP_001845.3:p.Pro902=
NM_080630.4:c.2356C=	NP_542197.3:p.Pro786=
NR_134980.2:n.3064C=
NM_001190709.2:c.2587C=	NP_001177638.1:p.Pro863=
NM_080629.3:c.2740C=	NP_542196.2:p.Pro914=