Canonical Allele Identifier: CA1185278435

Gene: COL11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.102993962C= , CM000663.2:g.102993962C=	GRCh38
NC_000001.10:g.103459518C= , CM000663.1:g.103459518C=	GRCh37
NC_000001.9:g.103232106C=	NCBI36
NG_008033.1:g.119535G=
NG_008033.2:g.119535G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370096.9:c.2340+1902G= MANE Select	ENSP00000359114.3:n.2340+1902G=
ENST00000353414.8:c.2223+1902G=	ENSP00000302551.6:n.2223+1902G=
ENST00000358392.6:c.2376+1902G=	ENSP00000351163.2:n.2376+1902G=
ENST00000370096.7:c.2340+1902G=	ENSP00000359114.3:n.2340+1902G=
ENST00000512756.5:c.1992+1902G=	ENSP00000426533.1:n.1992+1902G=
ENST00000635193.1:c.1658+1902G=
NM_001190709.1:c.2223+1902G=	NP_001177638.1:n.2223+1902G=
NM_001854.3:c.2340+1902G=	NP_001845.3:n.2340+1902G=
NM_080629.2:c.2376+1902G=	NP_542196.2:n.2376+1902G=
NM_080630.3:c.1992+1902G=	NP_542197.3:n.1992+1902G=
XM_011540719.1:c.2340+1902G=	XP_011539021.1:n.2340+1902G=
XM_011540720.1:c.573+1902G=	XP_011539022.1:n.573+1902G=
XM_011540721.1:c.-89+1902G=	XP_011539023.1:n.-89+1902G=
XR_946545.1:n.2738+1902G=
NR_134980.1:n.2658+1902G=
XM_017000334.1:c.2493+1902G=	XP_016855823.1:n.2493+1902G=
XM_017000335.1:c.2487+1902G=	XP_016855824.1:n.2487+1902G=
XM_017000336.1:c.2493+1902G=	XP_016855825.1:n.2493+1902G=
XM_017000337.1:c.891+1902G=	XP_016855826.1:n.891+1902G=
NM_001854.4:c.2340+1902G= MANE Select	NP_001845.3:n.2340+1902G=
NM_080630.4:c.1992+1902G=	NP_542197.3:n.1992+1902G=
NR_134980.2:n.2684+1902G=
NM_001190709.2:c.2223+1902G=	NP_001177638.1:n.2223+1902G=
NM_080629.3:c.2376+1902G=	NP_542196.2:n.2376+1902G=