Canonical Allele Identifier: CA351196642

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238280480A>C (hg19) ; chr2:g.237371837A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237371837A>C , CM000664.2:g.237371837A>C	GRCh38
NC_000002.11:g.238280480A>C , CM000664.1:g.238280480A>C	GRCh37
NC_000002.10:g.237945219A>C	NCBI36
NG_008676.1:g.47371T>G , LRG_473:g.47371T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.3562T>G	ENSP00000315873.4:p.Phe1188Val
ENST00000684597.1:c.11T>G
ENST00000295550.9:c.4180T>G MANE Select	ENSP00000295550.4:p.Phe1394Val
ENST00000295550.8:c.4180T>G	ENSP00000295550.4:p.Phe1394Val
ENST00000347401.7:c.2359T>G	ENSP00000315609.4:p.Phe787Val
ENST00000353578.8:c.3562T>G	ENSP00000315873.4:p.Phe1188Val
ENST00000392003.6:c.2959T>G	ENSP00000375860.2:p.Phe987Val
ENST00000392004.7:c.3562T>G	ENSP00000375861.3:p.Phe1188Val
ENST00000409809.5:c.3562T>G	ENSP00000386844.1:p.Phe1188Val
ENST00000472056.5:c.2359T>G	ENSP00000418285.1:p.Phe787Val
NM_004369.3:c.4180T>G , LRG_473t1:c.4180T>G	NP_004360.2:p.Phe1394Val
NM_057164.4:c.2959T>G	NP_476505.3:p.Phe987Val
NM_057165.4:c.3562T>G	NP_476506.3:p.Phe1188Val
NM_057166.4:c.2359T>G	NP_476507.3:p.Phe787Val
NM_057167.3:c.3562T>G	NP_476508.2:p.Phe1188Val
XM_005246065.1:c.3580T>G	XP_005246122.1:p.Phe1194Val
XM_005246066.1:c.2959T>G	XP_005246123.1:p.Phe987Val
XM_006712253.1:c.4180T>G	XP_006712316.1:p.Phe1394Val
XM_011510574.1:c.4180T>G	XP_011508876.1:p.Phe1394Val
XM_011510575.1:c.1774T>G	XP_011508877.1:p.Phe592Val
XM_017003304.1:c.1774T>G	XP_016858793.1:p.Phe592Val
XM_024452684.1:c.2959T>G	XP_024308452.1:p.Phe987Val
NM_004369.4:c.4180T>G MANE Select	NP_004360.2:p.Phe1394Val
NM_057164.5:c.2959T>G	NP_476505.3:p.Phe987Val
NM_057165.5:c.3562T>G	NP_476506.3:p.Phe1188Val
NM_057166.5:c.2359T>G	NP_476507.3:p.Phe787Val
NM_057167.4:c.3562T>G	NP_476508.2:p.Phe1188Val