Canonical Allele Identifier: CA1619889836

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164434C= , CM000668.2:g.33164434C=	GRCh38
NC_000006.11:g.33132211C= , CM000668.1:g.33132211C=	GRCh37
NC_000006.10:g.33240189C=	NCBI36
NG_011589.1:g.33035G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.709G=
ENST00000341947.7:c.4903G= MANE Select	ENSP00000339915.2:p.Val1635=
ENST00000341947.6:c.4903G=	ENSP00000339915.2:p.Val1635=
ENST00000361917.5:c.4582G=	ENSP00000355123.1:p.Val1528=
ENST00000374708.8:c.4645G=	ENSP00000363840.4:p.Val1549=
ENST00000477772.1:n.693G=
NM_080679.2:c.4582G=	NP_542410.2:p.Val1528=
NM_080680.2:c.4903G=	NP_542411.2:p.Val1635=
NM_080681.2:c.4645G=	NP_542412.2:p.Val1549=
XM_011514298.1:c.4057G=	XP_011512600.1:p.Val1353=
XM_011514299.1:c.4189G=	XP_011512601.1:p.Val1397=
XM_011514300.1:c.4009G=	XP_011512602.1:p.Val1337=
XM_011514301.1:c.3946G=	XP_011512603.1:p.Val1316=
XM_011514302.1:c.3790G=	XP_011512604.1:p.Val1264=
XM_011514299.2:c.4189G=	XP_011512601.1:p.Val1397=
XM_011514300.2:c.4009G=	XP_011512602.1:p.Val1337=
XM_011514302.2:c.3790G=	XP_011512604.1:p.Val1264=
XM_017010250.1:c.4903G=	XP_016865739.1:p.Val1635=
XM_017010251.2:c.3721G=	XP_016865740.1:p.Val1241=
NM_080680.3:c.4903G= MANE Select	NP_542411.2:p.Val1635=
NM_080681.3:c.4645G=	NP_542412.2:p.Val1549=
NM_080679.3:c.4582G=	NP_542410.2:p.Val1528=