Canonical Allele Identifier: CA351191681

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244987G>T (hg19) ; chr2:g.237336344G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336344G>T , CM000664.2:g.237336344G>T	GRCh38
NC_000002.11:g.238244987G>T , CM000664.1:g.238244987G>T	GRCh37
NC_000002.10:g.237909726G>T	NCBI36
NG_008676.1:g.82864C>A , LRG_473:g.82864C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1401C>A
ENST00000353578.9:c.8138C>A	ENSP00000315873.4:p.Ala2713Asp
ENST00000682957.1:c.883C>A
ENST00000684508.1:n.1023C>A
ENST00000295550.9:c.8756C>A MANE Select	ENSP00000295550.4:p.Ala2919Asp
ENST00000295550.8:c.8756C>A	ENSP00000295550.4:p.Ala2919Asp
ENST00000347401.7:c.6932C>A	ENSP00000315609.4:p.Ala2311Asp
ENST00000353578.8:c.8138C>A	ENSP00000315873.4:p.Ala2713Asp
ENST00000409809.5:c.8138C>A	ENSP00000386844.1:p.Ala2713Asp
ENST00000472056.5:c.6935C>A	ENSP00000418285.1:p.Ala2312Asp
ENST00000491769.1:n.5198C>A
NM_004369.3:c.8756C>A , LRG_473t1:c.8756C>A	NP_004360.2:p.Ala2919Asp
NM_057166.4:c.6935C>A	NP_476507.3:p.Ala2312Asp
NM_057167.3:c.8138C>A	NP_476508.2:p.Ala2713Asp
XM_005246065.1:c.8156C>A	XP_005246122.1:p.Ala2719Asp
XM_005246066.1:c.7535C>A	XP_005246123.1:p.Ala2512Asp
XM_006712253.1:c.8255C>A	XP_006712316.1:p.Ala2752Asp
XM_011510574.1:c.8753C>A	XP_011508876.1:p.Ala2918Asp
XM_011510575.1:c.6350C>A	XP_011508877.1:p.Ala2117Asp
XM_017003304.1:c.6350C>A	XP_016858793.1:p.Ala2117Asp
XM_024452684.1:c.7535C>A	XP_024308452.1:p.Ala2512Asp
NM_004369.4:c.8756C>A MANE Select	NP_004360.2:p.Ala2919Asp
NM_057166.5:c.6935C>A	NP_476507.3:p.Ala2312Asp
NM_057167.4:c.8138C>A	NP_476508.2:p.Ala2713Asp