Canonical Allele Identifier: CA1619889865

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164451C= , CM000668.2:g.33164451C=	GRCh38
NC_000006.11:g.33132228C= , CM000668.1:g.33132228C=	GRCh37
NC_000006.10:g.33240206C=	NCBI36
NG_011589.1:g.33018G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.692G=
ENST00000341947.7:c.4886G= MANE Select	ENSP00000339915.2:p.Gly1629=
ENST00000341947.6:c.4886G=	ENSP00000339915.2:p.Gly1629=
ENST00000361917.5:c.4565G=	ENSP00000355123.1:p.Gly1522=
ENST00000374708.8:c.4628G=	ENSP00000363840.4:p.Gly1543=
ENST00000477772.1:n.676G=
NM_080679.2:c.4565G=	NP_542410.2:p.Gly1522=
NM_080680.2:c.4886G=	NP_542411.2:p.Gly1629=
NM_080681.2:c.4628G=	NP_542412.2:p.Gly1543=
XM_011514298.1:c.4040G=	XP_011512600.1:p.Gly1347=
XM_011514299.1:c.4172G=	XP_011512601.1:p.Gly1391=
XM_011514300.1:c.3992G=	XP_011512602.1:p.Gly1331=
XM_011514301.1:c.3929G=	XP_011512603.1:p.Gly1310=
XM_011514302.1:c.3773G=	XP_011512604.1:p.Gly1258=
XM_011514299.2:c.4172G=	XP_011512601.1:p.Gly1391=
XM_011514300.2:c.3992G=	XP_011512602.1:p.Gly1331=
XM_011514302.2:c.3773G=	XP_011512604.1:p.Gly1258=
XM_017010250.1:c.4886G=	XP_016865739.1:p.Gly1629=
XM_017010251.2:c.3704G=	XP_016865740.1:p.Gly1235=
NM_080680.3:c.4886G= MANE Select	NP_542411.2:p.Gly1629=
NM_080681.3:c.4628G=	NP_542412.2:p.Gly1543=
NM_080679.3:c.4565G=	NP_542410.2:p.Gly1522=