Canonical Allele Identifier: CA1619890613

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164951G= , CM000668.2:g.33164951G=	GRCh38
NC_000006.11:g.33132728G= , CM000668.1:g.33132728G=	GRCh37
NC_000006.10:g.33240706G=	NCBI36
NG_011589.1:g.32518C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.570C=
ENST00000341947.7:c.4764C= MANE Select	ENSP00000339915.2:p.Val1588=
ENST00000341947.6:c.4764C=	ENSP00000339915.2:p.Val1588=
ENST00000361917.5:c.4443C=	ENSP00000355123.1:p.Val1481=
ENST00000374708.8:c.4506C=	ENSP00000363840.4:p.Val1502=
ENST00000477772.1:n.554C=
NM_080679.2:c.4443C=	NP_542410.2:p.Val1481=
NM_080680.2:c.4764C=	NP_542411.2:p.Val1588=
NM_080681.2:c.4506C=	NP_542412.2:p.Val1502=
XM_011514298.1:c.3918C=	XP_011512600.1:p.Val1306=
XM_011514299.1:c.4050C=	XP_011512601.1:p.Val1350=
XM_011514300.1:c.3870C=	XP_011512602.1:p.Val1290=
XM_011514301.1:c.3807C=	XP_011512603.1:p.Val1269=
XM_011514302.1:c.3651C=	XP_011512604.1:p.Val1217=
XM_011514299.2:c.4050C=	XP_011512601.1:p.Val1350=
XM_011514300.2:c.3870C=	XP_011512602.1:p.Val1290=
XM_011514302.2:c.3651C=	XP_011512604.1:p.Val1217=
XM_017010250.1:c.4764C=	XP_016865739.1:p.Val1588=
XM_017010251.2:c.3582C=	XP_016865740.1:p.Val1194=
NM_080680.3:c.4764C= MANE Select	NP_542411.2:p.Val1588=
NM_080681.3:c.4506C=	NP_542412.2:p.Val1502=
NM_080679.3:c.4443C=	NP_542410.2:p.Val1481=