Canonical Allele Identifier: CA1619889641

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164337C= , CM000668.2:g.33164337C=	GRCh38
NC_000006.11:g.33132114C= , CM000668.1:g.33132114C=	GRCh37
NC_000006.10:g.33240092C=	NCBI36
NG_011589.1:g.33132G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.806G=
ENST00000341947.7:c.5000G= MANE Select	ENSP00000339915.2:p.Arg1667=
ENST00000341947.6:c.5000G=	ENSP00000339915.2:p.Arg1667=
ENST00000361917.5:c.4679G=	ENSP00000355123.1:p.Arg1560=
ENST00000374708.8:c.4742G=	ENSP00000363840.4:p.Arg1581=
ENST00000477772.1:n.790G=
NM_080679.2:c.4679G=	NP_542410.2:p.Arg1560=
NM_080680.2:c.5000G=	NP_542411.2:p.Arg1667=
NM_080681.2:c.4742G=	NP_542412.2:p.Arg1581=
XM_011514298.1:c.4154G=	XP_011512600.1:p.Arg1385=
XM_011514299.1:c.4286G=	XP_011512601.1:p.Arg1429=
XM_011514300.1:c.4106G=	XP_011512602.1:p.Arg1369=
XM_011514301.1:c.4043G=	XP_011512603.1:p.Arg1348=
XM_011514302.1:c.3887G=	XP_011512604.1:p.Arg1296=
XM_011514299.2:c.4286G=	XP_011512601.1:p.Arg1429=
XM_011514300.2:c.4106G=	XP_011512602.1:p.Arg1369=
XM_011514302.2:c.3887G=	XP_011512604.1:p.Arg1296=
XM_017010250.1:c.5000G=	XP_016865739.1:p.Arg1667=
XM_017010251.2:c.3818G=	XP_016865740.1:p.Arg1273=
NM_080680.3:c.5000G= MANE Select	NP_542411.2:p.Arg1667=
NM_080681.3:c.4742G=	NP_542412.2:p.Arg1581=
NM_080679.3:c.4679G=	NP_542410.2:p.Arg1560=