Canonical Allele Identifier: CA363616053

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132115G>C (hg19) ; chr6:g.33164338G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164338G>C , CM000668.2:g.33164338G>C	GRCh38
NC_000006.11:g.33132115G>C , CM000668.1:g.33132115G>C	GRCh37
NC_000006.10:g.33240093G>C	NCBI36
NG_011589.1:g.33131C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.805C>G
ENST00000341947.7:c.4999C>G MANE Select	ENSP00000339915.2:p.Arg1667Gly
ENST00000341947.6:c.4999C>G	ENSP00000339915.2:p.Arg1667Gly
ENST00000361917.5:c.4678C>G	ENSP00000355123.1:p.Arg1560Gly
ENST00000374708.8:c.4741C>G	ENSP00000363840.4:p.Arg1581Gly
ENST00000477772.1:n.789C>G
NM_080679.2:c.4678C>G	NP_542410.2:p.Arg1560Gly
NM_080680.2:c.4999C>G	NP_542411.2:p.Arg1667Gly
NM_080681.2:c.4741C>G	NP_542412.2:p.Arg1581Gly
XM_011514298.1:c.4153C>G	XP_011512600.1:p.Arg1385Gly
XM_011514299.1:c.4285C>G	XP_011512601.1:p.Arg1429Gly
XM_011514300.1:c.4105C>G	XP_011512602.1:p.Arg1369Gly
XM_011514301.1:c.4042C>G	XP_011512603.1:p.Arg1348Gly
XM_011514302.1:c.3886C>G	XP_011512604.1:p.Arg1296Gly
XM_011514299.2:c.4285C>G	XP_011512601.1:p.Arg1429Gly
XM_011514300.2:c.4105C>G	XP_011512602.1:p.Arg1369Gly
XM_011514302.2:c.3886C>G	XP_011512604.1:p.Arg1296Gly
XM_017010250.1:c.4999C>G	XP_016865739.1:p.Arg1667Gly
XM_017010251.2:c.3817C>G	XP_016865740.1:p.Arg1273Gly
NM_080680.3:c.4999C>G MANE Select	NP_542411.2:p.Arg1667Gly
NM_080681.3:c.4741C>G	NP_542412.2:p.Arg1581Gly
NM_080679.3:c.4678C>G	NP_542410.2:p.Arg1560Gly