Canonical Allele Identifier: CA1185260613

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102961880G= , CM000663.2:g.102961880G=	GRCh38
NC_000001.10:g.103427436G= , CM000663.1:g.103427436G=	GRCh37
NC_000001.9:g.103200024G=	NCBI36
NG_008033.1:g.151617C=
NG_008033.2:g.151617C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3154C= MANE Select	ENSP00000359114.3:p.Pro1052=
ENST00000353414.8:c.3037C=	ENSP00000302551.6:p.Pro1013=
ENST00000358392.6:c.3190C=	ENSP00000351163.2:p.Pro1064=
ENST00000370096.7:c.3154C=	ENSP00000359114.3:p.Pro1052=
ENST00000465209.1:n.162C=
ENST00000512756.5:c.2806C=	ENSP00000426533.1:p.Pro936=
ENST00000635193.1:c.2488C=
NM_001190709.1:c.3037C=	NP_001177638.1:p.Pro1013=
NM_001854.3:c.3154C=	NP_001845.3:p.Pro1052=
NM_080629.2:c.3190C=	NP_542196.2:p.Pro1064=
NM_080630.3:c.2806C=	NP_542197.3:p.Pro936=
XM_011540719.1:c.3154C=	XP_011539021.1:p.Pro1052=
XM_011540720.1:c.1387C=	XP_011539022.1:p.Pro463=
XM_011540721.1:c.742C=	XP_011539023.1:p.Pro248=
NR_134980.1:n.3488C=
XM_017000334.1:c.3307C=	XP_016855823.1:p.Pro1103=
XM_017000335.1:c.3301C=	XP_016855824.1:p.Pro1101=
XM_017000336.1:c.3307C=	XP_016855825.1:p.Pro1103=
XM_017000337.1:c.1705C=	XP_016855826.1:p.Pro569=
NM_001854.4:c.3154C= MANE Select	NP_001845.3:p.Pro1052=
NM_080630.4:c.2806C=	NP_542197.3:p.Pro936=
NR_134980.2:n.3514C=
NM_001190709.2:c.3037C=	NP_001177638.1:p.Pro1013=
NM_080629.3:c.3190C=	NP_542196.2:p.Pro1064=