Canonical Allele Identifier: CA1619889879

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164457G= , CM000668.2:g.33164457G=	GRCh38
NC_000006.11:g.33132234G= , CM000668.1:g.33132234G=	GRCh37
NC_000006.10:g.33240212G=	NCBI36
NG_011589.1:g.33012C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.686C=
ENST00000341947.7:c.4880C= MANE Select	ENSP00000339915.2:p.Ser1627=
ENST00000341947.6:c.4880C=	ENSP00000339915.2:p.Ser1627=
ENST00000361917.5:c.4559C=	ENSP00000355123.1:p.Ser1520=
ENST00000374708.8:c.4622C=	ENSP00000363840.4:p.Ser1541=
ENST00000477772.1:n.670C=
NM_080679.2:c.4559C=	NP_542410.2:p.Ser1520=
NM_080680.2:c.4880C=	NP_542411.2:p.Ser1627=
NM_080681.2:c.4622C=	NP_542412.2:p.Ser1541=
XM_011514298.1:c.4034C=	XP_011512600.1:p.Ser1345=
XM_011514299.1:c.4166C=	XP_011512601.1:p.Ser1389=
XM_011514300.1:c.3986C=	XP_011512602.1:p.Ser1329=
XM_011514301.1:c.3923C=	XP_011512603.1:p.Ser1308=
XM_011514302.1:c.3767C=	XP_011512604.1:p.Ser1256=
XM_011514299.2:c.4166C=	XP_011512601.1:p.Ser1389=
XM_011514300.2:c.3986C=	XP_011512602.1:p.Ser1329=
XM_011514302.2:c.3767C=	XP_011512604.1:p.Ser1256=
XM_017010250.1:c.4880C=	XP_016865739.1:p.Ser1627=
XM_017010251.2:c.3698C=	XP_016865740.1:p.Ser1233=
NM_080680.3:c.4880C= MANE Select	NP_542411.2:p.Ser1627=
NM_080681.3:c.4622C=	NP_542412.2:p.Ser1541=
NM_080679.3:c.4559C=	NP_542410.2:p.Ser1520=