Canonical Allele Identifier: CA1619889773

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164398C= , CM000668.2:g.33164398C=	GRCh38
NC_000006.11:g.33132175C= , CM000668.1:g.33132175C=	GRCh37
NC_000006.10:g.33240153C=	NCBI36
NG_011589.1:g.33071G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.745G=
ENST00000341947.7:c.4939G= MANE Select	ENSP00000339915.2:p.Ala1647=
ENST00000341947.6:c.4939G=	ENSP00000339915.2:p.Ala1647=
ENST00000361917.5:c.4618G=	ENSP00000355123.1:p.Ala1540=
ENST00000374708.8:c.4681G=	ENSP00000363840.4:p.Ala1561=
ENST00000477772.1:n.729G=
NM_080679.2:c.4618G=	NP_542410.2:p.Ala1540=
NM_080680.2:c.4939G=	NP_542411.2:p.Ala1647=
NM_080681.2:c.4681G=	NP_542412.2:p.Ala1561=
XM_011514298.1:c.4093G=	XP_011512600.1:p.Ala1365=
XM_011514299.1:c.4225G=	XP_011512601.1:p.Ala1409=
XM_011514300.1:c.4045G=	XP_011512602.1:p.Ala1349=
XM_011514301.1:c.3982G=	XP_011512603.1:p.Ala1328=
XM_011514302.1:c.3826G=	XP_011512604.1:p.Ala1276=
XM_011514299.2:c.4225G=	XP_011512601.1:p.Ala1409=
XM_011514300.2:c.4045G=	XP_011512602.1:p.Ala1349=
XM_011514302.2:c.3826G=	XP_011512604.1:p.Ala1276=
XM_017010250.1:c.4939G=	XP_016865739.1:p.Ala1647=
XM_017010251.2:c.3757G=	XP_016865740.1:p.Ala1253=
NM_080680.3:c.4939G= MANE Select	NP_542411.2:p.Ala1647=
NM_080681.3:c.4681G=	NP_542412.2:p.Ala1561=
NM_080679.3:c.4618G=	NP_542410.2:p.Ala1540=