Canonical Allele Identifier: CA1619890415

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164859A= , CM000668.2:g.33164859A=	GRCh38
NC_000006.11:g.33132636A= , CM000668.1:g.33132636A=	GRCh37
NC_000006.10:g.33240614A=	NCBI36
NG_011589.1:g.32610T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000683572.1:n.662T=
ENST00000341947.7:c.4856T= MANE Select	ENSP00000339915.2:p.Val1619=
ENST00000341947.6:c.4856T=	ENSP00000339915.2:p.Val1619=
ENST00000361917.5:c.4535T=	ENSP00000355123.1:p.Val1512=
ENST00000374708.8:c.4598T=	ENSP00000363840.4:p.Val1533=
ENST00000477772.1:n.646T=
NM_080679.2:c.4535T=	NP_542410.2:p.Val1512=
NM_080680.2:c.4856T=	NP_542411.2:p.Val1619=
NM_080681.2:c.4598T=	NP_542412.2:p.Val1533=
XM_011514298.1:c.4010T=	XP_011512600.1:p.Val1337=
XM_011514299.1:c.4142T=	XP_011512601.1:p.Val1381=
XM_011514300.1:c.3962T=	XP_011512602.1:p.Val1321=
XM_011514301.1:c.3899T=	XP_011512603.1:p.Val1300=
XM_011514302.1:c.3743T=	XP_011512604.1:p.Val1248=
XM_011514299.2:c.4142T=	XP_011512601.1:p.Val1381=
XM_011514300.2:c.3962T=	XP_011512602.1:p.Val1321=
XM_011514302.2:c.3743T=	XP_011512604.1:p.Val1248=
XM_017010250.1:c.4856T=	XP_016865739.1:p.Val1619=
XM_017010251.2:c.3674T=	XP_016865740.1:p.Val1225=
NM_080680.3:c.4856T= MANE Select	NP_542411.2:p.Val1619=
NM_080681.3:c.4598T=	NP_542412.2:p.Val1533=
NM_080679.3:c.4535T=	NP_542410.2:p.Val1512=