Canonical Allele Identifier: CA1619889858

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164447G= , CM000668.2:g.33164447G=	GRCh38
NC_000006.11:g.33132224G= , CM000668.1:g.33132224G=	GRCh37
NC_000006.10:g.33240202G=	NCBI36
NG_011589.1:g.33022C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.696C=
ENST00000341947.7:c.4890C= MANE Select	ENSP00000339915.2:p.Ser1630=
ENST00000341947.6:c.4890C=	ENSP00000339915.2:p.Ser1630=
ENST00000361917.5:c.4569C=	ENSP00000355123.1:p.Ser1523=
ENST00000374708.8:c.4632C=	ENSP00000363840.4:p.Ser1544=
ENST00000477772.1:n.680C=
NM_080679.2:c.4569C=	NP_542410.2:p.Ser1523=
NM_080680.2:c.4890C=	NP_542411.2:p.Ser1630=
NM_080681.2:c.4632C=	NP_542412.2:p.Ser1544=
XM_011514298.1:c.4044C=	XP_011512600.1:p.Ser1348=
XM_011514299.1:c.4176C=	XP_011512601.1:p.Ser1392=
XM_011514300.1:c.3996C=	XP_011512602.1:p.Ser1332=
XM_011514301.1:c.3933C=	XP_011512603.1:p.Ser1311=
XM_011514302.1:c.3777C=	XP_011512604.1:p.Ser1259=
XM_011514299.2:c.4176C=	XP_011512601.1:p.Ser1392=
XM_011514300.2:c.3996C=	XP_011512602.1:p.Ser1332=
XM_011514302.2:c.3777C=	XP_011512604.1:p.Ser1259=
XM_017010250.1:c.4890C=	XP_016865739.1:p.Ser1630=
XM_017010251.2:c.3708C=	XP_016865740.1:p.Ser1236=
NM_080680.3:c.4890C= MANE Select	NP_542411.2:p.Ser1630=
NM_080681.3:c.4632C=	NP_542412.2:p.Ser1544=
NM_080679.3:c.4569C=	NP_542410.2:p.Ser1523=