Canonical Allele Identifier: CA1619889691

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164361G= , CM000668.2:g.33164361G=	GRCh38
NC_000006.11:g.33132138G= , CM000668.1:g.33132138G=	GRCh37
NC_000006.10:g.33240116G=	NCBI36
NG_011589.1:g.33108C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.782C=
ENST00000341947.7:c.4976C= MANE Select	ENSP00000339915.2:p.Ala1659=
ENST00000341947.6:c.4976C=	ENSP00000339915.2:p.Ala1659=
ENST00000361917.5:c.4655C=	ENSP00000355123.1:p.Ala1552=
ENST00000374708.8:c.4718C=	ENSP00000363840.4:p.Ala1573=
ENST00000477772.1:n.766C=
NM_080679.2:c.4655C=	NP_542410.2:p.Ala1552=
NM_080680.2:c.4976C=	NP_542411.2:p.Ala1659=
NM_080681.2:c.4718C=	NP_542412.2:p.Ala1573=
XM_011514298.1:c.4130C=	XP_011512600.1:p.Ala1377=
XM_011514299.1:c.4262C=	XP_011512601.1:p.Ala1421=
XM_011514300.1:c.4082C=	XP_011512602.1:p.Ala1361=
XM_011514301.1:c.4019C=	XP_011512603.1:p.Ala1340=
XM_011514302.1:c.3863C=	XP_011512604.1:p.Ala1288=
XM_011514299.2:c.4262C=	XP_011512601.1:p.Ala1421=
XM_011514300.2:c.4082C=	XP_011512602.1:p.Ala1361=
XM_011514302.2:c.3863C=	XP_011512604.1:p.Ala1288=
XM_017010250.1:c.4976C=	XP_016865739.1:p.Ala1659=
XM_017010251.2:c.3794C=	XP_016865740.1:p.Ala1265=
NM_080680.3:c.4976C= MANE Select	NP_542411.2:p.Ala1659=
NM_080681.3:c.4718C=	NP_542412.2:p.Ala1573=
NM_080679.3:c.4655C=	NP_542410.2:p.Ala1552=