Canonical Allele Identifier: CA1619896024

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33169459T= , CM000668.2:g.33169459T=	GRCh38
NC_000006.11:g.33137236T= , CM000668.1:g.33137236T=	GRCh37
NC_000006.10:g.33245214T=	NCBI36
NG_011589.1:g.28010A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341947.7:c.3722A= MANE Select	ENSP00000339915.2:p.Glu1241=
ENST00000341947.6:c.3722A=	ENSP00000339915.2:p.Glu1241=
ENST00000361917.5:c.3401A=	ENSP00000355123.1:p.Glu1134=
ENST00000374708.8:c.3464A=	ENSP00000363840.4:p.Glu1155=
ENST00000477772.1:n.273-3643A=
NM_080679.2:c.3401A=	NP_542410.2:p.Glu1134=
NM_080680.2:c.3722A=	NP_542411.2:p.Glu1241=
NM_080681.2:c.3464A=	NP_542412.2:p.Glu1155=
XM_011514298.1:c.2876A=	XP_011512600.1:p.Glu959=
XM_011514299.1:c.3008A=	XP_011512601.1:p.Glu1003=
XM_011514300.1:c.2828A=	XP_011512602.1:p.Glu943=
XM_011514301.1:c.2765A=	XP_011512603.1:p.Glu922=
XM_011514302.1:c.2609A=	XP_011512604.1:p.Glu870=
XM_011514299.2:c.3008A=	XP_011512601.1:p.Glu1003=
XM_011514300.2:c.2828A=	XP_011512602.1:p.Glu943=
XM_011514302.2:c.2609A=	XP_011512604.1:p.Glu870=
XM_017010250.1:c.3722A=	XP_016865739.1:p.Glu1241=
XM_017010251.2:c.2540A=	XP_016865740.1:p.Glu847=
NM_080680.3:c.3722A= MANE Select	NP_542411.2:p.Glu1241=
NM_080681.3:c.3464A=	NP_542412.2:p.Glu1155=
NM_080679.3:c.3401A=	NP_542410.2:p.Glu1134=