Canonical Allele Identifier: CA1337607261

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336541A= , CM000664.2:g.237336541A=	GRCh38
NC_000002.11:g.238245184A= , CM000664.1:g.238245184A=	GRCh37
NC_000002.10:g.237909923A=	NCBI36
NG_008676.1:g.82667T= , LRG_473:g.82667T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1213-9T=
ENST00000353578.9:c.7950-9T=	ENSP00000315873.4:n.7950-9T=
ENST00000682957.1:c.695-9T=
ENST00000684508.1:n.835-9T=
ENST00000295550.9:c.8568-9T= MANE Select	ENSP00000295550.4:n.8568-9T=
ENST00000295550.8:c.8568-9T=	ENSP00000295550.4:n.8568-9T=
ENST00000347401.7:c.6744-9T=	ENSP00000315609.4:n.6744-9T=
ENST00000353578.8:c.7950-9T=	ENSP00000315873.4:n.7950-9T=
ENST00000409809.5:c.7950-9T=	ENSP00000386844.1:n.7950-9T=
ENST00000472056.5:c.6747-9T=	ENSP00000418285.1:n.6747-9T=
ENST00000491769.1:n.5010-9T=
NM_004369.3:c.8568-9T= , LRG_473t1:c.8568-9T=	NP_004360.2:n.8568-9T=
NM_057166.4:c.6747-9T=	NP_476507.3:n.6747-9T=
NM_057167.3:c.7950-9T=	NP_476508.2:n.7950-9T=
XM_005246065.1:c.7968-9T=	XP_005246122.1:n.7968-9T=
XM_005246066.1:c.7347-9T=	XP_005246123.1:n.7347-9T=
XM_006712253.1:c.8067-9T=	XP_006712316.1:n.8067-9T=
XM_011510574.1:c.8565-9T=	XP_011508876.1:n.8565-9T=
XM_011510575.1:c.6162-9T=	XP_011508877.1:n.6162-9T=
XM_017003304.1:c.6162-9T=	XP_016858793.1:n.6162-9T=
XM_024452684.1:c.7347-9T=	XP_024308452.1:n.7347-9T=
NM_004369.4:c.8568-9T= MANE Select	NP_004360.2:n.8568-9T=
NM_057166.5:c.6747-9T=	NP_476507.3:n.6747-9T=
NM_057167.4:c.7950-9T=	NP_476508.2:n.7950-9T=