Canonical Allele Identifier: CA1619889680

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164355T= , CM000668.2:g.33164355T=	GRCh38
NC_000006.11:g.33132132T= , CM000668.1:g.33132132T=	GRCh37
NC_000006.10:g.33240110T=	NCBI36
NG_011589.1:g.33114A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.788A=
ENST00000341947.7:c.4982A= MANE Select	ENSP00000339915.2:p.Asp1661=
ENST00000341947.6:c.4982A=	ENSP00000339915.2:p.Asp1661=
ENST00000361917.5:c.4661A=	ENSP00000355123.1:p.Asp1554=
ENST00000374708.8:c.4724A=	ENSP00000363840.4:p.Asp1575=
ENST00000477772.1:n.772A=
NM_080679.2:c.4661A=	NP_542410.2:p.Asp1554=
NM_080680.2:c.4982A=	NP_542411.2:p.Asp1661=
NM_080681.2:c.4724A=	NP_542412.2:p.Asp1575=
XM_011514298.1:c.4136A=	XP_011512600.1:p.Asp1379=
XM_011514299.1:c.4268A=	XP_011512601.1:p.Asp1423=
XM_011514300.1:c.4088A=	XP_011512602.1:p.Asp1363=
XM_011514301.1:c.4025A=	XP_011512603.1:p.Asp1342=
XM_011514302.1:c.3869A=	XP_011512604.1:p.Asp1290=
XM_011514299.2:c.4268A=	XP_011512601.1:p.Asp1423=
XM_011514300.2:c.4088A=	XP_011512602.1:p.Asp1363=
XM_011514302.2:c.3869A=	XP_011512604.1:p.Asp1290=
XM_017010250.1:c.4982A=	XP_016865739.1:p.Asp1661=
XM_017010251.2:c.3800A=	XP_016865740.1:p.Asp1267=
NM_080680.3:c.4982A= MANE Select	NP_542411.2:p.Asp1661=
NM_080681.3:c.4724A=	NP_542412.2:p.Asp1575=
NM_080679.3:c.4661A=	NP_542410.2:p.Asp1554=