Canonical Allele Identifier: CA2187419

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336208C>T , CM000664.2:g.237336208C>T	GRCh38
NC_000002.11:g.238244851C>T , CM000664.1:g.238244851C>T	GRCh37
NC_000002.10:g.237909590C>T	NCBI36
NG_008676.1:g.83000G>A , LRG_473:g.83000G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1537G>A
ENST00000353578.9:c.8274G>A	ENSP00000315873.4:p.Ala2758=
ENST00000682957.1:c.1019G>A
ENST00000684508.1:n.1159G>A
ENST00000295550.9:c.8892G>A MANE Select	ENSP00000295550.4:p.Ala2964=
ENST00000295550.8:c.8892G>A	ENSP00000295550.4:p.Ala2964=
ENST00000347401.7:c.7068G>A	ENSP00000315609.4:p.Ala2356=
ENST00000353578.8:c.8274G>A	ENSP00000315873.4:p.Ala2758=
ENST00000409809.5:c.8274G>A	ENSP00000386844.1:p.Ala2758=
ENST00000472056.5:c.7071G>A	ENSP00000418285.1:p.Ala2357=
ENST00000491769.1:n.5334G>A
NM_004369.3:c.8892G>A , LRG_473t1:c.8892G>A	NP_004360.2:p.Ala2964=
NM_057166.4:c.7071G>A	NP_476507.3:p.Ala2357=
NM_057167.3:c.8274G>A	NP_476508.2:p.Ala2758=
XM_005246065.1:c.8292G>A	XP_005246122.1:p.Ala2764=
XM_005246066.1:c.7671G>A	XP_005246123.1:p.Ala2557=
XM_006712253.1:c.8391G>A	XP_006712316.1:p.Ala2797=
XM_011510574.1:c.8889G>A	XP_011508876.1:p.Ala2963=
XM_011510575.1:c.6486G>A	XP_011508877.1:p.Ala2162=
XM_017003304.1:c.6486G>A	XP_016858793.1:p.Ala2162=
XM_024452684.1:c.7671G>A	XP_024308452.1:p.Ala2557=
NM_004369.4:c.8892G>A MANE Select	NP_004360.2:p.Ala2964=
NM_057166.5:c.7071G>A	NP_476507.3:p.Ala2357=
NM_057167.4:c.8274G>A	NP_476508.2:p.Ala2758=