Canonical Allele Identifier: CA2188507

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237363324G>A , CM000664.2:g.237363324G>A	GRCh38
NC_000002.11:g.238271967G>A , CM000664.1:g.238271967G>A	GRCh37
NC_000002.10:g.237936706G>A	NCBI36
NG_008676.1:g.55884C>T , LRG_473:g.55884C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.5992C>T MANE Select	NP_004360.2:p.Arg1998Ter
ENST00000295550.9:c.5992C>T MANE Select	ENSP00000295550.4:p.Arg1998Ter
NM_004369.3:c.5992C>T , LRG_473t1:c.5992C>T	NP_004360.2:p.Arg1998Ter
NM_057166.4:c.4171C>T	NP_476507.3:p.Arg1391Ter
NM_057166.5:c.4171C>T	NP_476507.3:p.Arg1391Ter
NM_057167.3:c.5374C>T	NP_476508.2:p.Arg1792Ter
NM_057167.4:c.5374C>T	NP_476508.2:p.Arg1792Ter
ENST00000295550.8:c.5992C>T	ENSP00000295550.4:p.Arg1998Ter
ENST00000347401.7:c.4171C>T	ENSP00000315609.4:p.Arg1391Ter
ENST00000353578.8:c.5374C>T	ENSP00000315873.4:p.Arg1792Ter
ENST00000353578.9:c.5374C>T	ENSP00000315873.4:p.Arg1792Ter
ENST00000409809.5:c.5374C>T	ENSP00000386844.1:p.Arg1792Ter
ENST00000472056.5:c.4171C>T	ENSP00000418285.1:p.Arg1391Ter
XM_005246065.1:c.5392C>T	XP_005246122.1:p.Arg1798Ter
XM_005246066.1:c.4771C>T	XP_005246123.1:p.Arg1591Ter
XM_006712253.1:c.5491C>T	XP_006712316.1:p.Arg1831Ter
XM_011510574.1:c.5989C>T	XP_011508876.1:p.Arg1997Ter
XM_011510575.1:c.3586C>T	XP_011508877.1:p.Arg1196Ter
XM_017003304.1:c.3586C>T	XP_016858793.1:p.Arg1196Ter
XM_024452684.1:c.4771C>T	XP_024308452.1:p.Arg1591Ter