Canonical Allele Identifier: CA1619889667

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164350G= , CM000668.2:g.33164350G=	GRCh38
NC_000006.11:g.33132127G= , CM000668.1:g.33132127G=	GRCh37
NC_000006.10:g.33240105G=	NCBI36
NG_011589.1:g.33119C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.793C=
ENST00000341947.7:c.4987C= MANE Select	ENSP00000339915.2:p.Pro1663=
ENST00000341947.6:c.4987C=	ENSP00000339915.2:p.Pro1663=
ENST00000361917.5:c.4666C=	ENSP00000355123.1:p.Pro1556=
ENST00000374708.8:c.4729C=	ENSP00000363840.4:p.Pro1577=
ENST00000477772.1:n.777C=
NM_080679.2:c.4666C=	NP_542410.2:p.Pro1556=
NM_080680.2:c.4987C=	NP_542411.2:p.Pro1663=
NM_080681.2:c.4729C=	NP_542412.2:p.Pro1577=
XM_011514298.1:c.4141C=	XP_011512600.1:p.Pro1381=
XM_011514299.1:c.4273C=	XP_011512601.1:p.Pro1425=
XM_011514300.1:c.4093C=	XP_011512602.1:p.Pro1365=
XM_011514301.1:c.4030C=	XP_011512603.1:p.Pro1344=
XM_011514302.1:c.3874C=	XP_011512604.1:p.Pro1292=
XM_011514299.2:c.4273C=	XP_011512601.1:p.Pro1425=
XM_011514300.2:c.4093C=	XP_011512602.1:p.Pro1365=
XM_011514302.2:c.3874C=	XP_011512604.1:p.Pro1292=
XM_017010250.1:c.4987C=	XP_016865739.1:p.Pro1663=
XM_017010251.2:c.3805C=	XP_016865740.1:p.Pro1269=
NM_080680.3:c.4987C= MANE Select	NP_542411.2:p.Pro1663=
NM_080681.3:c.4729C=	NP_542412.2:p.Pro1577=
NM_080679.3:c.4666C=	NP_542410.2:p.Pro1556=