Canonical Allele Identifier: CA1337617822

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237360131C= , CM000664.2:g.237360131C=	GRCh38
NC_000002.11:g.238268774C= , CM000664.1:g.238268774C=	GRCh37
NC_000002.10:g.237933513C=	NCBI36
NG_008676.1:g.59077G= , LRG_473:g.59077G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.5621G=	ENSP00000315873.4:p.Gly1874=
ENST00000295550.9:c.6239G= MANE Select	ENSP00000295550.4:p.Gly2080=
ENST00000295550.8:c.6239G=	ENSP00000295550.4:p.Gly2080=
ENST00000347401.7:c.4418G=	ENSP00000315609.4:p.Gly1473=
ENST00000353578.8:c.5621G=	ENSP00000315873.4:p.Gly1874=
ENST00000409809.5:c.5621G=	ENSP00000386844.1:p.Gly1874=
ENST00000472056.5:c.4418G=	ENSP00000418285.1:p.Gly1473=
NM_004369.3:c.6239G= , LRG_473t1:c.6239G=	NP_004360.2:p.Gly2080=
NM_057166.4:c.4418G=	NP_476507.3:p.Gly1473=
NM_057167.3:c.5621G=	NP_476508.2:p.Gly1874=
XM_005246065.1:c.5639G=	XP_005246122.1:p.Gly1880=
XM_005246066.1:c.5018G=	XP_005246123.1:p.Gly1673=
XM_006712253.1:c.5738G=	XP_006712316.1:p.Gly1913=
XM_011510574.1:c.6236G=	XP_011508876.1:p.Gly2079=
XM_011510575.1:c.3833G=	XP_011508877.1:p.Gly1278=
XM_017003304.1:c.3833G=	XP_016858793.1:p.Gly1278=
XM_024452684.1:c.5018G=	XP_024308452.1:p.Gly1673=
NM_004369.4:c.6239G= MANE Select	NP_004360.2:p.Gly2080=
NM_057166.5:c.4418G=	NP_476507.3:p.Gly1473=
NM_057167.4:c.5621G=	NP_476508.2:p.Gly1874=