Canonical Allele Identifier: CA2189296

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237376940C>T , CM000664.2:g.237376940C>T	GRCh38
NC_000002.11:g.238285583C>T , CM000664.1:g.238285583C>T	GRCh37
NC_000002.10:g.237950322C>T	NCBI36
NG_008676.1:g.42268G>A , LRG_473:g.42268G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.2902G>A MANE Select	NP_004360.2:p.Val968Ile
ENST00000295550.9:c.2902G>A MANE Select	ENSP00000295550.4:p.Val968Ile
NM_004369.3:c.2902G>A , LRG_473t1:c.2902G>A	NP_004360.2:p.Val968Ile
NM_057164.4:c.1681G>A	NP_476505.3:p.Val561Ile
NM_057164.5:c.1681G>A	NP_476505.3:p.Val561Ile
NM_057165.4:c.2284G>A	NP_476506.3:p.Val762Ile
NM_057165.5:c.2284G>A	NP_476506.3:p.Val762Ile
NM_057166.4:c.1081G>A	NP_476507.3:p.Val361Ile
NM_057166.5:c.1081G>A	NP_476507.3:p.Val361Ile
NM_057167.3:c.2284G>A	NP_476508.2:p.Val762Ile
NM_057167.4:c.2284G>A	NP_476508.2:p.Val762Ile
ENST00000295550.8:c.2902G>A	ENSP00000295550.4:p.Val968Ile
ENST00000347401.7:c.1081G>A	ENSP00000315609.4:p.Val361Ile
ENST00000353578.8:c.2284G>A	ENSP00000315873.4:p.Val762Ile
ENST00000353578.9:c.2284G>A	ENSP00000315873.4:p.Val762Ile
ENST00000392003.6:c.1681G>A	ENSP00000375860.2:p.Val561Ile
ENST00000392004.7:c.2284G>A	ENSP00000375861.3:p.Val762Ile
ENST00000409809.5:c.2284G>A	ENSP00000386844.1:p.Val762Ile
ENST00000472056.5:c.1081G>A	ENSP00000418285.1:p.Val361Ile
XM_005246065.1:c.2302G>A	XP_005246122.1:p.Val768Ile
XM_005246066.1:c.1681G>A	XP_005246123.1:p.Val561Ile
XM_006712253.1:c.2902G>A	XP_006712316.1:p.Val968Ile
XM_011510574.1:c.2902G>A	XP_011508876.1:p.Val968Ile
XM_011510575.1:c.496G>A	XP_011508877.1:p.Val166Ile
XM_017003304.1:c.496G>A	XP_016858793.1:p.Val166Ile
XM_024452684.1:c.1681G>A	XP_024308452.1:p.Val561Ile