Canonical Allele Identifier: CA449867321

Gene: COL11A2

Linked Data

• gnomAD v4: 6-33164936-G-T
• MyVariant Identifiers: chr6:g.33132713G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33164936G>T , CM000668.2:g.33164936G>T	GRCh38
NC_000006.11:g.33132713G>T , CM000668.1:g.33132713G>T	GRCh37
NC_000006.10:g.33240691G>T	NCBI36
NG_011589.1:g.32533C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683572.1:n.585C>A
ENST00000341947.7:c.4779C>A MANE Select	ENSP00000339915.2:p.Gly1593=
ENST00000341947.6:c.4779C>A	ENSP00000339915.2:p.Gly1593=
ENST00000361917.5:c.4458C>A	ENSP00000355123.1:p.Gly1486=
ENST00000374708.8:c.4521C>A	ENSP00000363840.4:p.Gly1507=
ENST00000477772.1:n.569C>A
NM_080679.2:c.4458C>A	NP_542410.2:p.Gly1486=
NM_080680.2:c.4779C>A	NP_542411.2:p.Gly1593=
NM_080681.2:c.4521C>A	NP_542412.2:p.Gly1507=
XM_011514298.1:c.3933C>A	XP_011512600.1:p.Gly1311=
XM_011514299.1:c.4065C>A	XP_011512601.1:p.Gly1355=
XM_011514300.1:c.3885C>A	XP_011512602.1:p.Gly1295=
XM_011514301.1:c.3822C>A	XP_011512603.1:p.Gly1274=
XM_011514302.1:c.3666C>A	XP_011512604.1:p.Gly1222=
XM_011514299.2:c.4065C>A	XP_011512601.1:p.Gly1355=
XM_011514300.2:c.3885C>A	XP_011512602.1:p.Gly1295=
XM_011514302.2:c.3666C>A	XP_011512604.1:p.Gly1222=
XM_017010250.1:c.4779C>A	XP_016865739.1:p.Gly1593=
XM_017010251.2:c.3597C>A	XP_016865740.1:p.Gly1199=
NM_080680.3:c.4779C>A MANE Select	NP_542411.2:p.Gly1593=
NM_080681.3:c.4521C>A	NP_542412.2:p.Gly1507=
NM_080679.3:c.4458C>A	NP_542410.2:p.Gly1486=