Canonical Allele Identifier: CA449867243

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132641A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164864A>G , CM000668.2:g.33164864A>G	GRCh38
NC_000006.11:g.33132641A>G , CM000668.1:g.33132641A>G	GRCh37
NC_000006.10:g.33240619A>G	NCBI36
NG_011589.1:g.32605T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000683572.1:n.657T>C
ENST00000341947.7:c.4851T>C MANE Select	ENSP00000339915.2:p.Asp1617=
ENST00000341947.6:c.4851T>C	ENSP00000339915.2:p.Asp1617=
ENST00000361917.5:c.4530T>C	ENSP00000355123.1:p.Asp1510=
ENST00000374708.8:c.4593T>C	ENSP00000363840.4:p.Asp1531=
ENST00000477772.1:n.641T>C
NM_080679.2:c.4530T>C	NP_542410.2:p.Asp1510=
NM_080680.2:c.4851T>C	NP_542411.2:p.Asp1617=
NM_080681.2:c.4593T>C	NP_542412.2:p.Asp1531=
XM_011514298.1:c.4005T>C	XP_011512600.1:p.Asp1335=
XM_011514299.1:c.4137T>C	XP_011512601.1:p.Asp1379=
XM_011514300.1:c.3957T>C	XP_011512602.1:p.Asp1319=
XM_011514301.1:c.3894T>C	XP_011512603.1:p.Asp1298=
XM_011514302.1:c.3738T>C	XP_011512604.1:p.Asp1246=
XM_011514299.2:c.4137T>C	XP_011512601.1:p.Asp1379=
XM_011514300.2:c.3957T>C	XP_011512602.1:p.Asp1319=
XM_011514302.2:c.3738T>C	XP_011512604.1:p.Asp1246=
XM_017010250.1:c.4851T>C	XP_016865739.1:p.Asp1617=
XM_017010251.2:c.3669T>C	XP_016865740.1:p.Asp1223=
NM_080680.3:c.4851T>C MANE Select	NP_542411.2:p.Asp1617=
NM_080681.3:c.4593T>C	NP_542412.2:p.Asp1531=
NM_080679.3:c.4530T>C	NP_542410.2:p.Asp1510=