Canonical Allele Identifier: CA1619890522

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164916C= , CM000668.2:g.33164916C=	GRCh38
NC_000006.11:g.33132693C= , CM000668.1:g.33132693C=	GRCh37
NC_000006.10:g.33240671C=	NCBI36
NG_011589.1:g.32553G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.605G=
ENST00000341947.7:c.4799G= MANE Select	ENSP00000339915.2:p.Arg1600=
ENST00000341947.6:c.4799G=	ENSP00000339915.2:p.Arg1600=
ENST00000361917.5:c.4478G=	ENSP00000355123.1:p.Arg1493=
ENST00000374708.8:c.4541G=	ENSP00000363840.4:p.Arg1514=
ENST00000477772.1:n.589G=
NM_080679.2:c.4478G=	NP_542410.2:p.Arg1493=
NM_080680.2:c.4799G=	NP_542411.2:p.Arg1600=
NM_080681.2:c.4541G=	NP_542412.2:p.Arg1514=
XM_011514298.1:c.3953G=	XP_011512600.1:p.Arg1318=
XM_011514299.1:c.4085G=	XP_011512601.1:p.Arg1362=
XM_011514300.1:c.3905G=	XP_011512602.1:p.Arg1302=
XM_011514301.1:c.3842G=	XP_011512603.1:p.Arg1281=
XM_011514302.1:c.3686G=	XP_011512604.1:p.Arg1229=
XM_011514299.2:c.4085G=	XP_011512601.1:p.Arg1362=
XM_011514300.2:c.3905G=	XP_011512602.1:p.Arg1302=
XM_011514302.2:c.3686G=	XP_011512604.1:p.Arg1229=
XM_017010250.1:c.4799G=	XP_016865739.1:p.Arg1600=
XM_017010251.2:c.3617G=	XP_016865740.1:p.Arg1206=
NM_080680.3:c.4799G= MANE Select	NP_542411.2:p.Arg1600=
NM_080681.3:c.4541G=	NP_542412.2:p.Arg1514=
NM_080679.3:c.4478G=	NP_542410.2:p.Arg1493=