Canonical Allele Identifier: CA1337609711

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237342163T= , CM000664.2:g.237342163T=	GRCh38
NC_000002.11:g.238250806T= , CM000664.1:g.238250806T=	GRCh37
NC_000002.10:g.237915545T=	NCBI36
NG_008676.1:g.77045A= , LRG_473:g.77045A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.7669-2A= MANE Select	NP_004360.2:n.7669-2A=
ENST00000295550.9:c.7669-2A= MANE Select	ENSP00000295550.4:n.7669-2A=
NM_004369.3:c.7669-2A= , LRG_473t1:c.7669-2A=	NP_004360.2:n.7669-2A=
NM_057166.4:c.5848-2A=	NP_476507.3:n.5848-2A=
NM_057166.5:c.5848-2A=	NP_476507.3:n.5848-2A=
NM_057167.3:c.7051-2A=	NP_476508.2:n.7051-2A=
NM_057167.4:c.7051-2A=	NP_476508.2:n.7051-2A=
ENST00000295550.8:c.7669-2A=	ENSP00000295550.4:n.7669-2A=
ENST00000347401.7:c.5845-2A=	ENSP00000315609.4:n.5845-2A=
ENST00000347401.8:c.314-2A=
ENST00000353578.8:c.7051-2A=	ENSP00000315873.4:n.7051-2A=
ENST00000353578.9:c.7051-2A=	ENSP00000315873.4:n.7051-2A=
ENST00000409809.5:c.7051-2A=	ENSP00000386844.1:n.7051-2A=
ENST00000472056.5:c.5848-2A=	ENSP00000418285.1:n.5848-2A=
ENST00000491769.1:n.4109A=
XM_005246065.1:c.7069-2A=	XP_005246122.1:n.7069-2A=
XM_005246066.1:c.6448-2A=	XP_005246123.1:n.6448-2A=
XM_006712253.1:c.7168-2A=	XP_006712316.1:n.7168-2A=
XM_011510574.1:c.7666-2A=	XP_011508876.1:n.7666-2A=
XM_011510575.1:c.5263-2A=	XP_011508877.1:n.5263-2A=
XM_017003304.1:c.5263-2A=	XP_016858793.1:n.5263-2A=
XM_024452684.1:c.6448-2A=	XP_024308452.1:n.6448-2A=