Canonical Allele Identifier: CA2189283

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237376883C>T , CM000664.2:g.237376883C>T	GRCh38
NC_000002.11:g.238285526C>T , CM000664.1:g.238285526C>T	GRCh37
NC_000002.10:g.237950265C>T	NCBI36
NG_008676.1:g.42325G>A , LRG_473:g.42325G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.2959G>A MANE Select	NP_004360.2:p.Val987Met
ENST00000295550.9:c.2959G>A MANE Select	ENSP00000295550.4:p.Val987Met
NM_004369.3:c.2959G>A , LRG_473t1:c.2959G>A	NP_004360.2:p.Val987Met
NM_057164.4:c.1738G>A	NP_476505.3:p.Val580Met
NM_057164.5:c.1738G>A	NP_476505.3:p.Val580Met
NM_057165.4:c.2341G>A	NP_476506.3:p.Val781Met
NM_057165.5:c.2341G>A	NP_476506.3:p.Val781Met
NM_057166.4:c.1138G>A	NP_476507.3:p.Val380Met
NM_057166.5:c.1138G>A	NP_476507.3:p.Val380Met
NM_057167.3:c.2341G>A	NP_476508.2:p.Val781Met
NM_057167.4:c.2341G>A	NP_476508.2:p.Val781Met
ENST00000295550.8:c.2959G>A	ENSP00000295550.4:p.Val987Met
ENST00000347401.7:c.1138G>A	ENSP00000315609.4:p.Val380Met
ENST00000353578.8:c.2341G>A	ENSP00000315873.4:p.Val781Met
ENST00000353578.9:c.2341G>A	ENSP00000315873.4:p.Val781Met
ENST00000392003.6:c.1738G>A	ENSP00000375860.2:p.Val580Met
ENST00000392004.7:c.2341G>A	ENSP00000375861.3:p.Val781Met
ENST00000409809.5:c.2341G>A	ENSP00000386844.1:p.Val781Met
ENST00000472056.5:c.1138G>A	ENSP00000418285.1:p.Val380Met
XM_005246065.1:c.2359G>A	XP_005246122.1:p.Val787Met
XM_005246066.1:c.1738G>A	XP_005246123.1:p.Val580Met
XM_006712253.1:c.2959G>A	XP_006712316.1:p.Val987Met
XM_011510574.1:c.2959G>A	XP_011508876.1:p.Val987Met
XM_011510575.1:c.553G>A	XP_011508877.1:p.Val185Met
XM_017003304.1:c.553G>A	XP_016858793.1:p.Val185Met
XM_024452684.1:c.1738G>A	XP_024308452.1:p.Val580Met