Canonical Allele Identifier: CA1619889861

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164448G= , CM000668.2:g.33164448G=	GRCh38
NC_000006.11:g.33132225G= , CM000668.1:g.33132225G=	GRCh37
NC_000006.10:g.33240203G=	NCBI36
NG_011589.1:g.33021C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.695C=
ENST00000341947.7:c.4889C= MANE Select	ENSP00000339915.2:p.Ser1630=
ENST00000341947.6:c.4889C=	ENSP00000339915.2:p.Ser1630=
ENST00000361917.5:c.4568C=	ENSP00000355123.1:p.Ser1523=
ENST00000374708.8:c.4631C=	ENSP00000363840.4:p.Ser1544=
ENST00000477772.1:n.679C=
NM_080679.2:c.4568C=	NP_542410.2:p.Ser1523=
NM_080680.2:c.4889C=	NP_542411.2:p.Ser1630=
NM_080681.2:c.4631C=	NP_542412.2:p.Ser1544=
XM_011514298.1:c.4043C=	XP_011512600.1:p.Ser1348=
XM_011514299.1:c.4175C=	XP_011512601.1:p.Ser1392=
XM_011514300.1:c.3995C=	XP_011512602.1:p.Ser1332=
XM_011514301.1:c.3932C=	XP_011512603.1:p.Ser1311=
XM_011514302.1:c.3776C=	XP_011512604.1:p.Ser1259=
XM_011514299.2:c.4175C=	XP_011512601.1:p.Ser1392=
XM_011514300.2:c.3995C=	XP_011512602.1:p.Ser1332=
XM_011514302.2:c.3776C=	XP_011512604.1:p.Ser1259=
XM_017010250.1:c.4889C=	XP_016865739.1:p.Ser1630=
XM_017010251.2:c.3707C=	XP_016865740.1:p.Ser1236=
NM_080680.3:c.4889C= MANE Select	NP_542411.2:p.Ser1630=
NM_080681.3:c.4631C=	NP_542412.2:p.Ser1544=
NM_080679.3:c.4568C=	NP_542410.2:p.Ser1523=