Canonical Allele Identifier: CA2187849

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344826C>T , CM000664.2:g.237344826C>T	GRCh38
NC_000002.11:g.238253469C>T , CM000664.1:g.238253469C>T	GRCh37
NC_000002.10:g.237918208C>T	NCBI36
NG_008676.1:g.74382G>A , LRG_473:g.74382G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.7192G>A MANE Select	NP_004360.2:p.Val2398Ile
ENST00000295550.9:c.7192G>A MANE Select	ENSP00000295550.4:p.Val2398Ile
NM_004369.3:c.7192G>A , LRG_473t1:c.7192G>A	NP_004360.2:p.Val2398Ile
NM_057166.4:c.5371G>A	NP_476507.3:p.Val1791Ile
NM_057166.5:c.5371G>A	NP_476507.3:p.Val1791Ile
NM_057167.3:c.6574G>A	NP_476508.2:p.Val2192Ile
NM_057167.4:c.6574G>A	NP_476508.2:p.Val2192Ile
ENST00000295550.8:c.7192G>A	ENSP00000295550.4:p.Val2398Ile
ENST00000347401.7:c.5368G>A	ENSP00000315609.4:p.Val1790Ile
ENST00000353578.8:c.6574G>A	ENSP00000315873.4:p.Val2192Ile
ENST00000353578.9:c.6574G>A	ENSP00000315873.4:p.Val2192Ile
ENST00000409809.5:c.6574G>A	ENSP00000386844.1:p.Val2192Ile
ENST00000472056.5:c.5371G>A	ENSP00000418285.1:p.Val1791Ile
ENST00000491769.1:n.1446G>A
XM_005246065.1:c.6592G>A	XP_005246122.1:p.Val2198Ile
XM_005246066.1:c.5971G>A	XP_005246123.1:p.Val1991Ile
XM_006712253.1:c.6691G>A	XP_006712316.1:p.Val2231Ile
XM_011510574.1:c.7189G>A	XP_011508876.1:p.Val2397Ile
XM_011510575.1:c.4786G>A	XP_011508877.1:p.Val1596Ile
XM_017003304.1:c.4786G>A	XP_016858793.1:p.Val1596Ile
XM_024452684.1:c.5971G>A	XP_024308452.1:p.Val1991Ile