Canonical Allele Identifier: CA1619889807

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164419G= , CM000668.2:g.33164419G=	GRCh38
NC_000006.11:g.33132196G= , CM000668.1:g.33132196G=	GRCh37
NC_000006.10:g.33240174G=	NCBI36
NG_011589.1:g.33050C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.724C=
ENST00000341947.7:c.4918C= MANE Select	ENSP00000339915.2:p.Leu1640=
ENST00000341947.6:c.4918C=	ENSP00000339915.2:p.Leu1640=
ENST00000361917.5:c.4597C=	ENSP00000355123.1:p.Leu1533=
ENST00000374708.8:c.4660C=	ENSP00000363840.4:p.Leu1554=
ENST00000477772.1:n.708C=
NM_080679.2:c.4597C=	NP_542410.2:p.Leu1533=
NM_080680.2:c.4918C=	NP_542411.2:p.Leu1640=
NM_080681.2:c.4660C=	NP_542412.2:p.Leu1554=
XM_011514298.1:c.4072C=	XP_011512600.1:p.Leu1358=
XM_011514299.1:c.4204C=	XP_011512601.1:p.Leu1402=
XM_011514300.1:c.4024C=	XP_011512602.1:p.Leu1342=
XM_011514301.1:c.3961C=	XP_011512603.1:p.Leu1321=
XM_011514302.1:c.3805C=	XP_011512604.1:p.Leu1269=
XM_011514299.2:c.4204C=	XP_011512601.1:p.Leu1402=
XM_011514300.2:c.4024C=	XP_011512602.1:p.Leu1342=
XM_011514302.2:c.3805C=	XP_011512604.1:p.Leu1269=
XM_017010250.1:c.4918C=	XP_016865739.1:p.Leu1640=
XM_017010251.2:c.3736C=	XP_016865740.1:p.Leu1246=
NM_080680.3:c.4918C= MANE Select	NP_542411.2:p.Leu1640=
NM_080681.3:c.4660C=	NP_542412.2:p.Leu1554=
NM_080679.3:c.4597C=	NP_542410.2:p.Leu1533=