Canonical Allele Identifier: CA1185258653

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102946872G= , CM000663.2:g.102946872G=	GRCh38
NC_000001.10:g.103412428G= , CM000663.1:g.103412428G=	GRCh37
NC_000001.9:g.103185016G=	NCBI36
NG_008033.1:g.166625C=
NG_008033.2:g.166625C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.3253C= MANE Select	ENSP00000359114.3:p.Pro1085=
ENST00000353414.8:c.3136C=	ENSP00000302551.6:p.Pro1046=
ENST00000358392.6:c.3289C=	ENSP00000351163.2:p.Pro1097=
ENST00000370096.7:c.3253C=	ENSP00000359114.3:p.Pro1085=
ENST00000512756.5:c.2905C=	ENSP00000426533.1:p.Pro969=
ENST00000635193.1:c.2587C=
NM_001190709.1:c.3136C=	NP_001177638.1:p.Pro1046=
NM_001854.3:c.3253C=	NP_001845.3:p.Pro1085=
NM_080629.2:c.3289C=	NP_542196.2:p.Pro1097=
NM_080630.3:c.2905C=	NP_542197.3:p.Pro969=
XM_011540719.1:c.3253C=	XP_011539021.1:p.Pro1085=
XM_011540720.1:c.1486C=	XP_011539022.1:p.Pro496=
XM_011540721.1:c.841C=	XP_011539023.1:p.Pro281=
NR_134980.1:n.3587C=
XM_017000334.1:c.3406C=	XP_016855823.1:p.Pro1136=
XM_017000335.1:c.3400C=	XP_016855824.1:p.Pro1134=
XM_017000336.1:c.3406C=	XP_016855825.1:p.Pro1136=
XM_017000337.1:c.1804C=	XP_016855826.1:p.Pro602=
NM_001854.4:c.3253C= MANE Select	NP_001845.3:p.Pro1085=
NM_080630.4:c.2905C=	NP_542197.3:p.Pro969=
NR_134980.2:n.3613C=
NM_001190709.2:c.3136C=	NP_001177638.1:p.Pro1046=
NM_080629.3:c.3289C=	NP_542196.2:p.Pro1097=