Canonical Allele Identifier: CA2188634

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237365992G>T , CM000664.2:g.237365992G>T	GRCh38
NC_000002.11:g.238274635G>T , CM000664.1:g.238274635G>T	GRCh37
NC_000002.10:g.237939374G>T	NCBI36
NG_008676.1:g.53216C>A , LRG_473:g.53216C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.5544C>A MANE Select	NP_004360.2:p.Asp1848Glu
ENST00000295550.9:c.5544C>A MANE Select	ENSP00000295550.4:p.Asp1848Glu
NM_004369.3:c.5544C>A , LRG_473t1:c.5544C>A	NP_004360.2:p.Asp1848Glu
NM_057166.4:c.3723C>A	NP_476507.3:p.Asp1241Glu
NM_057166.5:c.3723C>A	NP_476507.3:p.Asp1241Glu
NM_057167.3:c.4926C>A	NP_476508.2:p.Asp1642Glu
NM_057167.4:c.4926C>A	NP_476508.2:p.Asp1642Glu
ENST00000295550.8:c.5544C>A	ENSP00000295550.4:p.Asp1848Glu
ENST00000347401.7:c.3723C>A	ENSP00000315609.4:p.Asp1241Glu
ENST00000353578.8:c.4926C>A	ENSP00000315873.4:p.Asp1642Glu
ENST00000353578.9:c.4926C>A	ENSP00000315873.4:p.Asp1642Glu
ENST00000409809.5:c.4926C>A	ENSP00000386844.1:p.Asp1642Glu
ENST00000472056.5:c.3723C>A	ENSP00000418285.1:p.Asp1241Glu
XM_005246065.1:c.4944C>A	XP_005246122.1:p.Asp1648Glu
XM_005246066.1:c.4323C>A	XP_005246123.1:p.Asp1441Glu
XM_006712253.1:c.5043C>A	XP_006712316.1:p.Asp1681Glu
XM_011510574.1:c.5541C>A	XP_011508876.1:p.Asp1847Glu
XM_011510575.1:c.3138C>A	XP_011508877.1:p.Asp1046Glu
XM_017003304.1:c.3138C>A	XP_016858793.1:p.Asp1046Glu
XM_024452684.1:c.4323C>A	XP_024308452.1:p.Asp1441Glu