Canonical Allele Identifier: CA1619896939

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33171161G= , CM000668.2:g.33171161G=	GRCh38
NC_000006.11:g.33138938G= , CM000668.1:g.33138938G=	GRCh37
NC_000006.10:g.33246916G=	NCBI36
NG_011589.1:g.26308C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341947.7:c.3319C= MANE Select	ENSP00000339915.2:p.Pro1107=
ENST00000341947.6:c.3319C=	ENSP00000339915.2:p.Pro1107=
ENST00000361917.5:c.2998C=	ENSP00000355123.1:p.Pro1000=
ENST00000374708.8:c.3061C=	ENSP00000363840.4:p.Pro1021=
ENST00000477772.1:n.273-5345C=
NM_080679.2:c.2998C=	NP_542410.2:p.Pro1000=
NM_080680.2:c.3319C=	NP_542411.2:p.Pro1107=
NM_080681.2:c.3061C=	NP_542412.2:p.Pro1021=
XM_011514298.1:c.2473C=	XP_011512600.1:p.Pro825=
XM_011514299.1:c.2605C=	XP_011512601.1:p.Pro869=
XM_011514300.1:c.2425C=	XP_011512602.1:p.Pro809=
XM_011514301.1:c.2362C=	XP_011512603.1:p.Pro788=
XM_011514302.1:c.2206C=	XP_011512604.1:p.Pro736=
XM_011514299.2:c.2605C=	XP_011512601.1:p.Pro869=
XM_011514300.2:c.2425C=	XP_011512602.1:p.Pro809=
XM_011514302.2:c.2206C=	XP_011512604.1:p.Pro736=
XM_017010250.1:c.3319C=	XP_016865739.1:p.Pro1107=
XM_017010251.2:c.2137C=	XP_016865740.1:p.Pro713=
NM_080680.3:c.3319C= MANE Select	NP_542411.2:p.Pro1107=
NM_080681.3:c.3061C=	NP_542412.2:p.Pro1021=
NM_080679.3:c.2998C=	NP_542410.2:p.Pro1000=