Canonical Allele Identifier: CA1185258628

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102946840A= , CM000663.2:g.102946840A=	GRCh38
NC_000001.10:g.103412396A= , CM000663.1:g.103412396A=	GRCh37
NC_000001.9:g.103184984A=	NCBI36
NG_008033.1:g.166657T=
NG_008033.2:g.166657T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3276+9T= MANE Select	ENSP00000359114.3:n.3276+9T=
ENST00000353414.8:c.3159+9T=	ENSP00000302551.6:n.3159+9T=
ENST00000358392.6:c.3312+9T=	ENSP00000351163.2:n.3312+9T=
ENST00000370096.7:c.3276+9T=	ENSP00000359114.3:n.3276+9T=
ENST00000512756.5:c.2928+9T=	ENSP00000426533.1:n.2928+9T=
ENST00000635193.1:c.2610+9T=
NM_001190709.1:c.3159+9T=	NP_001177638.1:n.3159+9T=
NM_001854.3:c.3276+9T=	NP_001845.3:n.3276+9T=
NM_080629.2:c.3312+9T=	NP_542196.2:n.3312+9T=
NM_080630.3:c.2928+9T=	NP_542197.3:n.2928+9T=
XM_011540719.1:c.3276+9T=	XP_011539021.1:n.3276+9T=
XM_011540720.1:c.1509+9T=	XP_011539022.1:n.1509+9T=
XM_011540721.1:c.864+9T=	XP_011539023.1:n.864+9T=
NR_134980.1:n.3610+9T=
XM_017000334.1:c.3429+9T=	XP_016855823.1:n.3429+9T=
XM_017000335.1:c.3423+9T=	XP_016855824.1:n.3423+9T=
XM_017000336.1:c.3429+9T=	XP_016855825.1:n.3429+9T=
XM_017000337.1:c.1827+9T=	XP_016855826.1:n.1827+9T=
NM_001854.4:c.3276+9T= MANE Select	NP_001845.3:n.3276+9T=
NM_080630.4:c.2928+9T=	NP_542197.3:n.2928+9T=
NR_134980.2:n.3636+9T=
NM_001190709.2:c.3159+9T=	NP_001177638.1:n.3159+9T=
NM_080629.3:c.3312+9T=	NP_542196.2:n.3312+9T=