Canonical Allele Identifier: CA1619890449

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164874G= , CM000668.2:g.33164874G=	GRCh38
NC_000006.11:g.33132651G= , CM000668.1:g.33132651G=	GRCh37
NC_000006.10:g.33240629G=	NCBI36
NG_011589.1:g.32595C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.647C=
ENST00000341947.7:c.4841C= MANE Select	ENSP00000339915.2:p.Thr1614=
ENST00000341947.6:c.4841C=	ENSP00000339915.2:p.Thr1614=
ENST00000361917.5:c.4520C=	ENSP00000355123.1:p.Thr1507=
ENST00000374708.8:c.4583C=	ENSP00000363840.4:p.Thr1528=
ENST00000477772.1:n.631C=
NM_080679.2:c.4520C=	NP_542410.2:p.Thr1507=
NM_080680.2:c.4841C=	NP_542411.2:p.Thr1614=
NM_080681.2:c.4583C=	NP_542412.2:p.Thr1528=
XM_011514298.1:c.3995C=	XP_011512600.1:p.Thr1332=
XM_011514299.1:c.4127C=	XP_011512601.1:p.Thr1376=
XM_011514300.1:c.3947C=	XP_011512602.1:p.Thr1316=
XM_011514301.1:c.3884C=	XP_011512603.1:p.Thr1295=
XM_011514302.1:c.3728C=	XP_011512604.1:p.Thr1243=
XM_011514299.2:c.4127C=	XP_011512601.1:p.Thr1376=
XM_011514300.2:c.3947C=	XP_011512602.1:p.Thr1316=
XM_011514302.2:c.3728C=	XP_011512604.1:p.Thr1243=
XM_017010250.1:c.4841C=	XP_016865739.1:p.Thr1614=
XM_017010251.2:c.3659C=	XP_016865740.1:p.Thr1220=
NM_080680.3:c.4841C= MANE Select	NP_542411.2:p.Thr1614=
NM_080681.3:c.4583C=	NP_542412.2:p.Thr1528=
NM_080679.3:c.4520C=	NP_542410.2:p.Thr1507=