Canonical Allele Identifier: CA1337608635

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237340570C= , CM000664.2:g.237340570C=	GRCh38
NC_000002.11:g.238249213C= , CM000664.1:g.238249213C=	GRCh37
NC_000002.10:g.237913952C=	NCBI36
NG_008676.1:g.78638G= , LRG_473:g.78638G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.991G=
ENST00000353578.9:c.7728G=	ENSP00000315873.4:p.Glu2576=
ENST00000682957.1:c.349G=
ENST00000684508.1:n.613G=
ENST00000295550.9:c.8346G= MANE Select	ENSP00000295550.4:p.Glu2782=
ENST00000295550.8:c.8346G=	ENSP00000295550.4:p.Glu2782=
ENST00000347401.7:c.6522G=	ENSP00000315609.4:p.Glu2174=
ENST00000353578.8:c.7728G=	ENSP00000315873.4:p.Glu2576=
ENST00000409809.5:c.7728G=	ENSP00000386844.1:p.Glu2576=
ENST00000468792.1:n.33G=
ENST00000472056.5:c.6525G=	ENSP00000418285.1:p.Glu2175=
ENST00000491769.1:n.4788G=
NM_004369.3:c.8346G= , LRG_473t1:c.8346G=	NP_004360.2:p.Glu2782=
NM_057166.4:c.6525G=	NP_476507.3:p.Glu2175=
NM_057167.3:c.7728G=	NP_476508.2:p.Glu2576=
XM_005246065.1:c.7746G=	XP_005246122.1:p.Glu2582=
XM_005246066.1:c.7125G=	XP_005246123.1:p.Glu2375=
XM_006712253.1:c.7845G=	XP_006712316.1:p.Glu2615=
XM_011510574.1:c.8343G=	XP_011508876.1:p.Glu2781=
XM_011510575.1:c.5940G=	XP_011508877.1:p.Glu1980=
XM_017003304.1:c.5940G=	XP_016858793.1:p.Glu1980=
XM_024452684.1:c.7125G=	XP_024308452.1:p.Glu2375=
NM_004369.4:c.8346G= MANE Select	NP_004360.2:p.Glu2782=
NM_057166.5:c.6525G=	NP_476507.3:p.Glu2175=
NM_057167.4:c.7728G=	NP_476508.2:p.Glu2576=