Canonical Allele Identifier: CA1337606356

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237334586A= , CM000664.2:g.237334586A=	GRCh38
NC_000002.11:g.238243229A= , CM000664.1:g.238243229A=	GRCh37
NC_000002.10:g.237907968A=	NCBI36
NG_008676.1:g.84622T= , LRG_473:g.84622T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000347401.8:c.1611-1038T=
ENST00000353578.9:c.8611+40T=	ENSP00000315873.4:n.8611+40T=
ENST00000682957.1:c.1356+40T=
ENST00000683348.1:c.97+40T=	ENSP00000508058.1:n.97+40T=
ENST00000295550.9:c.9229+40T= MANE Select	ENSP00000295550.4:n.9229+40T=
ENST00000295550.8:c.9229+40T=	ENSP00000295550.4:n.9229+40T=
ENST00000347401.7:c.7405+40T=	ENSP00000315609.4:n.7405+40T=
ENST00000353578.8:c.8611+40T=	ENSP00000315873.4:n.8611+40T=
ENST00000409809.5:c.8611+40T=	ENSP00000386844.1:n.8611+40T=
ENST00000472056.5:c.7408+40T=	ENSP00000418285.1:n.7408+40T=
ENST00000491769.1:n.5671+40T=
ENST00000493608.1:n.161+40T=
NM_004369.3:c.9229+40T= , LRG_473t1:c.9229+40T=	NP_004360.2:n.9229+40T=
NM_057166.4:c.7408+40T=	NP_476507.3:n.7408+40T=
NM_057167.3:c.8611+40T=	NP_476508.2:n.8611+40T=
XM_005246065.1:c.8629+40T=	XP_005246122.1:n.8629+40T=
XM_005246066.1:c.8008+40T=	XP_005246123.1:n.8008+40T=
XM_006712253.1:c.8728+40T=	XP_006712316.1:n.8728+40T=
XM_011510574.1:c.9226+40T=	XP_011508876.1:n.9226+40T=
XM_011510575.1:c.6823+40T=	XP_011508877.1:n.6823+40T=
XM_017003304.1:c.6823+40T=	XP_016858793.1:n.6823+40T=
XM_024452684.1:c.8008+40T=	XP_024308452.1:n.8008+40T=
NM_004369.4:c.9229+40T= MANE Select	NP_004360.2:n.9229+40T=
NM_057166.5:c.7408+40T=	NP_476507.3:n.7408+40T=
NM_057167.4:c.8611+40T=	NP_476508.2:n.8611+40T=