Canonical Allele Identifier: CA351191589

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244960G>C (hg19) ; chr2:g.237336317G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336317G>C , CM000664.2:g.237336317G>C	GRCh38
NC_000002.11:g.238244960G>C , CM000664.1:g.238244960G>C	GRCh37
NC_000002.10:g.237909699G>C	NCBI36
NG_008676.1:g.82891C>G , LRG_473:g.82891C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1428C>G
ENST00000353578.9:c.8165C>G	ENSP00000315873.4:p.Ala2722Gly
ENST00000682957.1:c.910C>G
ENST00000684508.1:n.1050C>G
ENST00000295550.9:c.8783C>G MANE Select	ENSP00000295550.4:p.Ala2928Gly
ENST00000295550.8:c.8783C>G	ENSP00000295550.4:p.Ala2928Gly
ENST00000347401.7:c.6959C>G	ENSP00000315609.4:p.Ala2320Gly
ENST00000353578.8:c.8165C>G	ENSP00000315873.4:p.Ala2722Gly
ENST00000409809.5:c.8165C>G	ENSP00000386844.1:p.Ala2722Gly
ENST00000472056.5:c.6962C>G	ENSP00000418285.1:p.Ala2321Gly
ENST00000491769.1:n.5225C>G
NM_004369.3:c.8783C>G , LRG_473t1:c.8783C>G	NP_004360.2:p.Ala2928Gly
NM_057166.4:c.6962C>G	NP_476507.3:p.Ala2321Gly
NM_057167.3:c.8165C>G	NP_476508.2:p.Ala2722Gly
XM_005246065.1:c.8183C>G	XP_005246122.1:p.Ala2728Gly
XM_005246066.1:c.7562C>G	XP_005246123.1:p.Ala2521Gly
XM_006712253.1:c.8282C>G	XP_006712316.1:p.Ala2761Gly
XM_011510574.1:c.8780C>G	XP_011508876.1:p.Ala2927Gly
XM_011510575.1:c.6377C>G	XP_011508877.1:p.Ala2126Gly
XM_017003304.1:c.6377C>G	XP_016858793.1:p.Ala2126Gly
XM_024452684.1:c.7562C>G	XP_024308452.1:p.Ala2521Gly
NM_004369.4:c.8783C>G MANE Select	NP_004360.2:p.Ala2928Gly
NM_057166.5:c.6962C>G	NP_476507.3:p.Ala2321Gly
NM_057167.4:c.8165C>G	NP_476508.2:p.Ala2722Gly