Canonical Allele Identifier: CA1619889675

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164354G= , CM000668.2:g.33164354G=	GRCh38
NC_000006.11:g.33132131G= , CM000668.1:g.33132131G=	GRCh37
NC_000006.10:g.33240109G=	NCBI36
NG_011589.1:g.33115C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.789C=
ENST00000341947.7:c.4983C= MANE Select	ENSP00000339915.2:p.Asp1661=
ENST00000341947.6:c.4983C=	ENSP00000339915.2:p.Asp1661=
ENST00000361917.5:c.4662C=	ENSP00000355123.1:p.Asp1554=
ENST00000374708.8:c.4725C=	ENSP00000363840.4:p.Asp1575=
ENST00000477772.1:n.773C=
NM_080679.2:c.4662C=	NP_542410.2:p.Asp1554=
NM_080680.2:c.4983C=	NP_542411.2:p.Asp1661=
NM_080681.2:c.4725C=	NP_542412.2:p.Asp1575=
XM_011514298.1:c.4137C=	XP_011512600.1:p.Asp1379=
XM_011514299.1:c.4269C=	XP_011512601.1:p.Asp1423=
XM_011514300.1:c.4089C=	XP_011512602.1:p.Asp1363=
XM_011514301.1:c.4026C=	XP_011512603.1:p.Asp1342=
XM_011514302.1:c.3870C=	XP_011512604.1:p.Asp1290=
XM_011514299.2:c.4269C=	XP_011512601.1:p.Asp1423=
XM_011514300.2:c.4089C=	XP_011512602.1:p.Asp1363=
XM_011514302.2:c.3870C=	XP_011512604.1:p.Asp1290=
XM_017010250.1:c.4983C=	XP_016865739.1:p.Asp1661=
XM_017010251.2:c.3801C=	XP_016865740.1:p.Asp1267=
NM_080680.3:c.4983C= MANE Select	NP_542411.2:p.Asp1661=
NM_080681.3:c.4725C=	NP_542412.2:p.Asp1575=
NM_080679.3:c.4662C=	NP_542410.2:p.Asp1554=