Canonical Allele Identifier: CA351191682

Gene: COL6A3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1401C>G
ENST00000353578.9:c.8138C>G	ENSP00000315873.4:p.Ala2713Gly
ENST00000682957.1:c.883C>G
ENST00000684508.1:n.1023C>G
ENST00000295550.9:c.8756C>G MANE Select	ENSP00000295550.4:p.Ala2919Gly
ENST00000295550.8:c.8756C>G	ENSP00000295550.4:p.Ala2919Gly
ENST00000347401.7:c.6932C>G	ENSP00000315609.4:p.Ala2311Gly
ENST00000353578.8:c.8138C>G	ENSP00000315873.4:p.Ala2713Gly
ENST00000409809.5:c.8138C>G	ENSP00000386844.1:p.Ala2713Gly
ENST00000472056.5:c.6935C>G	ENSP00000418285.1:p.Ala2312Gly
ENST00000491769.1:n.5198C>G
NM_004369.3:c.8756C>G , LRG_473t1:c.8756C>G	NP_004360.2:p.Ala2919Gly
NM_057166.4:c.6935C>G	NP_476507.3:p.Ala2312Gly
NM_057167.3:c.8138C>G	NP_476508.2:p.Ala2713Gly
XM_005246065.1:c.8156C>G	XP_005246122.1:p.Ala2719Gly
XM_005246066.1:c.7535C>G	XP_005246123.1:p.Ala2512Gly
XM_006712253.1:c.8255C>G	XP_006712316.1:p.Ala2752Gly
XM_011510574.1:c.8753C>G	XP_011508876.1:p.Ala2918Gly
XM_011510575.1:c.6350C>G	XP_011508877.1:p.Ala2117Gly
XM_017003304.1:c.6350C>G	XP_016858793.1:p.Ala2117Gly
XM_024452684.1:c.7535C>G	XP_024308452.1:p.Ala2512Gly
NM_004369.4:c.8756C>G MANE Select	NP_004360.2:p.Ala2919Gly
NM_057166.5:c.6935C>G	NP_476507.3:p.Ala2312Gly
NM_057167.4:c.8138C>G	NP_476508.2:p.Ala2713Gly