Canonical Allele Identifier: CA1337627391

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237381418C= , CM000664.2:g.237381418C=	GRCh38
NC_000002.11:g.238290061C= , CM000664.1:g.238290061C=	GRCh37
NC_000002.10:g.237954800C=	NCBI36
NG_008676.1:g.37790G= , LRG_473:g.37790G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000353578.9:c.776G=	ENSP00000315873.4:p.Arg259=
ENST00000682405.1:n.167G=
ENST00000295550.9:c.1394G= MANE Select	ENSP00000295550.4:p.Arg465=
ENST00000295550.8:c.1394G=	ENSP00000295550.4:p.Arg465=
ENST00000347401.7:c.173G=	ENSP00000315609.4:p.Arg58=
ENST00000353578.8:c.776G=	ENSP00000315873.4:p.Arg259=
ENST00000392003.6:c.173G=	ENSP00000375860.2:p.Arg58=
ENST00000392004.7:c.776G=	ENSP00000375861.3:p.Arg259=
ENST00000409809.5:c.776G=	ENSP00000386844.1:p.Arg259=
ENST00000433762.1:c.1394G=	ENSP00000389539.1:p.Arg465=
ENST00000472056.5:c.173G=	ENSP00000418285.1:p.Arg58=
NM_004369.3:c.1394G= , LRG_473t1:c.1394G=	NP_004360.2:p.Arg465=
NM_057164.4:c.173G=	NP_476505.3:p.Arg58=
NM_057165.4:c.776G=	NP_476506.3:p.Arg259=
NM_057166.4:c.173G=	NP_476507.3:p.Arg58=
NM_057167.3:c.776G=	NP_476508.2:p.Arg259=
XM_005246065.1:c.1394G=	XP_005246122.1:p.Arg465=
XM_005246066.1:c.173G=	XP_005246123.1:p.Arg58=
XM_006712253.1:c.1394G=	XP_006712316.1:p.Arg465=
XM_011510574.1:c.1394G=	XP_011508876.1:p.Arg465=
XM_011510575.1:c.92-4074G=	XP_011508877.1:n.92-4074G=
XM_017003304.1:c.92-4074G=	XP_016858793.1:n.92-4074G=
XM_024452684.1:c.173G=	XP_024308452.1:p.Arg58=
NM_004369.4:c.1394G= MANE Select	NP_004360.2:p.Arg465=
NM_057164.5:c.173G=	NP_476505.3:p.Arg58=
NM_057165.5:c.776G=	NP_476506.3:p.Arg259=
NM_057166.5:c.173G=	NP_476507.3:p.Arg58=
NM_057167.4:c.776G=	NP_476508.2:p.Arg259=