Canonical Allele Identifier: CA1619889733

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164385A= , CM000668.2:g.33164385A=	GRCh38
NC_000006.11:g.33132162A= , CM000668.1:g.33132162A=	GRCh37
NC_000006.10:g.33240140A=	NCBI36
NG_011589.1:g.33084T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.758T=
ENST00000341947.7:c.4952T= MANE Select	ENSP00000339915.2:p.Val1651=
ENST00000341947.6:c.4952T=	ENSP00000339915.2:p.Val1651=
ENST00000361917.5:c.4631T=	ENSP00000355123.1:p.Val1544=
ENST00000374708.8:c.4694T=	ENSP00000363840.4:p.Val1565=
ENST00000477772.1:n.742T=
NM_080679.2:c.4631T=	NP_542410.2:p.Val1544=
NM_080680.2:c.4952T=	NP_542411.2:p.Val1651=
NM_080681.2:c.4694T=	NP_542412.2:p.Val1565=
XM_011514298.1:c.4106T=	XP_011512600.1:p.Val1369=
XM_011514299.1:c.4238T=	XP_011512601.1:p.Val1413=
XM_011514300.1:c.4058T=	XP_011512602.1:p.Val1353=
XM_011514301.1:c.3995T=	XP_011512603.1:p.Val1332=
XM_011514302.1:c.3839T=	XP_011512604.1:p.Val1280=
XM_011514299.2:c.4238T=	XP_011512601.1:p.Val1413=
XM_011514300.2:c.4058T=	XP_011512602.1:p.Val1353=
XM_011514302.2:c.3839T=	XP_011512604.1:p.Val1280=
XM_017010250.1:c.4952T=	XP_016865739.1:p.Val1651=
XM_017010251.2:c.3770T=	XP_016865740.1:p.Val1257=
NM_080680.3:c.4952T= MANE Select	NP_542411.2:p.Val1651=
NM_080681.3:c.4694T=	NP_542412.2:p.Val1565=
NM_080679.3:c.4631T=	NP_542410.2:p.Val1544=