Canonical Allele Identifier: CA351189710

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238243532A>T (hg19) ; chr2:g.237334889A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237334889A>T , CM000664.2:g.237334889A>T	GRCh38
NC_000002.11:g.238243532A>T , CM000664.1:g.238243532A>T	GRCh37
NC_000002.10:g.237908271A>T	NCBI36
NG_008676.1:g.84319T>A , LRG_473:g.84319T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000347401.8:c.1610+1246T>A
ENST00000353578.9:c.8348T>A	ENSP00000315873.4:p.Val2783Asp
ENST00000682957.1:c.1093T>A
ENST00000295550.9:c.8966T>A MANE Select	ENSP00000295550.4:p.Val2989Asp
ENST00000295550.8:c.8966T>A	ENSP00000295550.4:p.Val2989Asp
ENST00000347401.7:c.7142T>A	ENSP00000315609.4:p.Val2381Asp
ENST00000353578.8:c.8348T>A	ENSP00000315873.4:p.Val2783Asp
ENST00000409809.5:c.8348T>A	ENSP00000386844.1:p.Val2783Asp
ENST00000472056.5:c.7145T>A	ENSP00000418285.1:p.Val2382Asp
ENST00000491769.1:n.5408T>A
NM_004369.3:c.8966T>A , LRG_473t1:c.8966T>A	NP_004360.2:p.Val2989Asp
NM_057166.4:c.7145T>A	NP_476507.3:p.Val2382Asp
NM_057167.3:c.8348T>A	NP_476508.2:p.Val2783Asp
XM_005246065.1:c.8366T>A	XP_005246122.1:p.Val2789Asp
XM_005246066.1:c.7745T>A	XP_005246123.1:p.Val2582Asp
XM_006712253.1:c.8465T>A	XP_006712316.1:p.Val2822Asp
XM_011510574.1:c.8963T>A	XP_011508876.1:p.Val2988Asp
XM_011510575.1:c.6560T>A	XP_011508877.1:p.Val2187Asp
XM_017003304.1:c.6560T>A	XP_016858793.1:p.Val2187Asp
XM_024452684.1:c.7745T>A	XP_024308452.1:p.Val2582Asp
NM_004369.4:c.8966T>A MANE Select	NP_004360.2:p.Val2989Asp
NM_057166.5:c.7145T>A	NP_476507.3:p.Val2382Asp
NM_057167.4:c.8348T>A	NP_476508.2:p.Val2783Asp