Canonical Allele Identifier: CA449867219

Gene: COL11A2

Linked Data

• MyVariant Identifiers: chr6:g.33132629C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164852C>T , CM000668.2:g.33164852C>T	GRCh38
NC_000006.11:g.33132629C>T , CM000668.1:g.33132629C>T	GRCh37
NC_000006.10:g.33240607C>T	NCBI36
NG_011589.1:g.32617G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000683572.1:n.669G>A
ENST00000341947.7:c.4863G>A MANE Select	ENSP00000339915.2:p.Gln1621=
ENST00000341947.6:c.4863G>A	ENSP00000339915.2:p.Gln1621=
ENST00000361917.5:c.4542G>A	ENSP00000355123.1:p.Gln1514=
ENST00000374708.8:c.4605G>A	ENSP00000363840.4:p.Gln1535=
ENST00000477772.1:n.653G>A
NM_080679.2:c.4542G>A	NP_542410.2:p.Gln1514=
NM_080680.2:c.4863G>A	NP_542411.2:p.Gln1621=
NM_080681.2:c.4605G>A	NP_542412.2:p.Gln1535=
XM_011514298.1:c.4017G>A	XP_011512600.1:p.Gln1339=
XM_011514299.1:c.4149G>A	XP_011512601.1:p.Gln1383=
XM_011514300.1:c.3969G>A	XP_011512602.1:p.Gln1323=
XM_011514301.1:c.3906G>A	XP_011512603.1:p.Gln1302=
XM_011514302.1:c.3750G>A	XP_011512604.1:p.Gln1250=
XM_011514299.2:c.4149G>A	XP_011512601.1:p.Gln1383=
XM_011514300.2:c.3969G>A	XP_011512602.1:p.Gln1323=
XM_011514302.2:c.3750G>A	XP_011512604.1:p.Gln1250=
XM_017010250.1:c.4863G>A	XP_016865739.1:p.Gln1621=
XM_017010251.2:c.3681G>A	XP_016865740.1:p.Gln1227=
NM_080680.3:c.4863G>A MANE Select	NP_542411.2:p.Gln1621=
NM_080681.3:c.4605G>A	NP_542412.2:p.Gln1535=
NM_080679.3:c.4542G>A	NP_542410.2:p.Gln1514=