Canonical Allele Identifier: CA1619890409

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164856G= , CM000668.2:g.33164856G=	GRCh38
NC_000006.11:g.33132633G= , CM000668.1:g.33132633G=	GRCh37
NC_000006.10:g.33240611G=	NCBI36
NG_011589.1:g.32613C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000683572.1:n.665C=
ENST00000341947.7:c.4859C= MANE Select	ENSP00000339915.2:p.Thr1620=
ENST00000341947.6:c.4859C=	ENSP00000339915.2:p.Thr1620=
ENST00000361917.5:c.4538C=	ENSP00000355123.1:p.Thr1513=
ENST00000374708.8:c.4601C=	ENSP00000363840.4:p.Thr1534=
ENST00000477772.1:n.649C=
NM_080679.2:c.4538C=	NP_542410.2:p.Thr1513=
NM_080680.2:c.4859C=	NP_542411.2:p.Thr1620=
NM_080681.2:c.4601C=	NP_542412.2:p.Thr1534=
XM_011514298.1:c.4013C=	XP_011512600.1:p.Thr1338=
XM_011514299.1:c.4145C=	XP_011512601.1:p.Thr1382=
XM_011514300.1:c.3965C=	XP_011512602.1:p.Thr1322=
XM_011514301.1:c.3902C=	XP_011512603.1:p.Thr1301=
XM_011514302.1:c.3746C=	XP_011512604.1:p.Thr1249=
XM_011514299.2:c.4145C=	XP_011512601.1:p.Thr1382=
XM_011514300.2:c.3965C=	XP_011512602.1:p.Thr1322=
XM_011514302.2:c.3746C=	XP_011512604.1:p.Thr1249=
XM_017010250.1:c.4859C=	XP_016865739.1:p.Thr1620=
XM_017010251.2:c.3677C=	XP_016865740.1:p.Thr1226=
NM_080680.3:c.4859C= MANE Select	NP_542411.2:p.Thr1620=
NM_080681.3:c.4601C=	NP_542412.2:p.Thr1534=
NM_080679.3:c.4538C=	NP_542410.2:p.Thr1513=