Canonical Allele Identifier: CA363617685

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132705C>G (hg19) ; chr6:g.33164928C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164928C>G , CM000668.2:g.33164928C>G	GRCh38
NC_000006.11:g.33132705C>G , CM000668.1:g.33132705C>G	GRCh37
NC_000006.10:g.33240683C>G	NCBI36
NG_011589.1:g.32541G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.593G>C
ENST00000341947.7:c.4787G>C MANE Select	ENSP00000339915.2:p.Arg1596Pro
ENST00000341947.6:c.4787G>C	ENSP00000339915.2:p.Arg1596Pro
ENST00000361917.5:c.4466G>C	ENSP00000355123.1:p.Arg1489Pro
ENST00000374708.8:c.4529G>C	ENSP00000363840.4:p.Arg1510Pro
ENST00000477772.1:n.577G>C
NM_080679.2:c.4466G>C	NP_542410.2:p.Arg1489Pro
NM_080680.2:c.4787G>C	NP_542411.2:p.Arg1596Pro
NM_080681.2:c.4529G>C	NP_542412.2:p.Arg1510Pro
XM_011514298.1:c.3941G>C	XP_011512600.1:p.Arg1314Pro
XM_011514299.1:c.4073G>C	XP_011512601.1:p.Arg1358Pro
XM_011514300.1:c.3893G>C	XP_011512602.1:p.Arg1298Pro
XM_011514301.1:c.3830G>C	XP_011512603.1:p.Arg1277Pro
XM_011514302.1:c.3674G>C	XP_011512604.1:p.Arg1225Pro
XM_011514299.2:c.4073G>C	XP_011512601.1:p.Arg1358Pro
XM_011514300.2:c.3893G>C	XP_011512602.1:p.Arg1298Pro
XM_011514302.2:c.3674G>C	XP_011512604.1:p.Arg1225Pro
XM_017010250.1:c.4787G>C	XP_016865739.1:p.Arg1596Pro
XM_017010251.2:c.3605G>C	XP_016865740.1:p.Arg1202Pro
NM_080680.3:c.4787G>C MANE Select	NP_542411.2:p.Arg1596Pro
NM_080681.3:c.4529G>C	NP_542412.2:p.Arg1510Pro
NM_080679.3:c.4466G>C	NP_542410.2:p.Arg1489Pro