Canonical Allele Identifier: CA1337619325

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237363374C= , CM000664.2:g.237363374C=	GRCh38
NC_000002.11:g.238272017C= , CM000664.1:g.238272017C=	GRCh37
NC_000002.10:g.237936756C=	NCBI36
NG_008676.1:g.55834G= , LRG_473:g.55834G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.5324G=	ENSP00000315873.4:p.Gly1775=
ENST00000295550.9:c.5942G= MANE Select	ENSP00000295550.4:p.Gly1981=
ENST00000295550.8:c.5942G=	ENSP00000295550.4:p.Gly1981=
ENST00000347401.7:c.4121G=	ENSP00000315609.4:p.Gly1374=
ENST00000353578.8:c.5324G=	ENSP00000315873.4:p.Gly1775=
ENST00000409809.5:c.5324G=	ENSP00000386844.1:p.Gly1775=
ENST00000472056.5:c.4121G=	ENSP00000418285.1:p.Gly1374=
NM_004369.3:c.5942G= , LRG_473t1:c.5942G=	NP_004360.2:p.Gly1981=
NM_057166.4:c.4121G=	NP_476507.3:p.Gly1374=
NM_057167.3:c.5324G=	NP_476508.2:p.Gly1775=
XM_005246065.1:c.5342G=	XP_005246122.1:p.Gly1781=
XM_005246066.1:c.4721G=	XP_005246123.1:p.Gly1574=
XM_006712253.1:c.5441G=	XP_006712316.1:p.Gly1814=
XM_011510574.1:c.5939G=	XP_011508876.1:p.Gly1980=
XM_011510575.1:c.3536G=	XP_011508877.1:p.Gly1179=
XM_017003304.1:c.3536G=	XP_016858793.1:p.Gly1179=
XM_024452684.1:c.4721G=	XP_024308452.1:p.Gly1574=
NM_004369.4:c.5942G= MANE Select	NP_004360.2:p.Gly1981=
NM_057166.5:c.4121G=	NP_476507.3:p.Gly1374=
NM_057167.4:c.5324G=	NP_476508.2:p.Gly1775=