Canonical Allele Identifier: CA1619896938

Gene: COL11A2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33171156T= , CM000668.2:g.33171156T=	GRCh38
NC_000006.11:g.33138933T= , CM000668.1:g.33138933T=	GRCh37
NC_000006.10:g.33246911T=	NCBI36
NG_011589.1:g.26313A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341947.7:c.3324A= MANE Select	ENSP00000339915.2:p.Gly1108=
ENST00000341947.6:c.3324A=	ENSP00000339915.2:p.Gly1108=
ENST00000361917.5:c.3003A=	ENSP00000355123.1:p.Gly1001=
ENST00000374708.8:c.3066A=	ENSP00000363840.4:p.Gly1022=
ENST00000477772.1:n.273-5340A=
NM_080679.2:c.3003A=	NP_542410.2:p.Gly1001=
NM_080680.2:c.3324A=	NP_542411.2:p.Gly1108=
NM_080681.2:c.3066A=	NP_542412.2:p.Gly1022=
XM_011514298.1:c.2478A=	XP_011512600.1:p.Gly826=
XM_011514299.1:c.2610A=	XP_011512601.1:p.Gly870=
XM_011514300.1:c.2430A=	XP_011512602.1:p.Gly810=
XM_011514301.1:c.2367A=	XP_011512603.1:p.Gly789=
XM_011514302.1:c.2211A=	XP_011512604.1:p.Gly737=
XM_011514299.2:c.2610A=	XP_011512601.1:p.Gly870=
XM_011514300.2:c.2430A=	XP_011512602.1:p.Gly810=
XM_011514302.2:c.2211A=	XP_011512604.1:p.Gly737=
XM_017010250.1:c.3324A=	XP_016865739.1:p.Gly1108=
XM_017010251.2:c.2142A=	XP_016865740.1:p.Gly714=
NM_080680.3:c.3324A= MANE Select	NP_542411.2:p.Gly1108=
NM_080681.3:c.3066A=	NP_542412.2:p.Gly1022=
NM_080679.3:c.3003A=	NP_542410.2:p.Gly1001=