Canonical Allele Identifier: CA351202604

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238253165A>C (hg19) ; chr2:g.237344522A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344522A>C , CM000664.2:g.237344522A>C	GRCh38
NC_000002.11:g.238253165A>C , CM000664.1:g.238253165A>C	GRCh37
NC_000002.10:g.237917904A>C	NCBI36
NG_008676.1:g.74686T>G , LRG_473:g.74686T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.141T>G
ENST00000353578.9:c.6878T>G	ENSP00000315873.4:p.Phe2293Cys
ENST00000295550.9:c.7496T>G MANE Select	ENSP00000295550.4:p.Phe2499Cys
ENST00000295550.8:c.7496T>G	ENSP00000295550.4:p.Phe2499Cys
ENST00000347401.7:c.5672T>G	ENSP00000315609.4:p.Phe1891Cys
ENST00000353578.8:c.6878T>G	ENSP00000315873.4:p.Phe2293Cys
ENST00000409809.5:c.6878T>G	ENSP00000386844.1:p.Phe2293Cys
ENST00000472056.5:c.5675T>G	ENSP00000418285.1:p.Phe1892Cys
ENST00000491769.1:n.1750T>G
NM_004369.3:c.7496T>G , LRG_473t1:c.7496T>G	NP_004360.2:p.Phe2499Cys
NM_057166.4:c.5675T>G	NP_476507.3:p.Phe1892Cys
NM_057167.3:c.6878T>G	NP_476508.2:p.Phe2293Cys
XM_005246065.1:c.6896T>G	XP_005246122.1:p.Phe2299Cys
XM_005246066.1:c.6275T>G	XP_005246123.1:p.Phe2092Cys
XM_006712253.1:c.6995T>G	XP_006712316.1:p.Phe2332Cys
XM_011510574.1:c.7493T>G	XP_011508876.1:p.Phe2498Cys
XM_011510575.1:c.5090T>G	XP_011508877.1:p.Phe1697Cys
XM_017003304.1:c.5090T>G	XP_016858793.1:p.Phe1697Cys
XM_024452684.1:c.6275T>G	XP_024308452.1:p.Phe2092Cys
NM_004369.4:c.7496T>G MANE Select	NP_004360.2:p.Phe2499Cys
NM_057166.5:c.5675T>G	NP_476507.3:p.Phe1892Cys
NM_057167.4:c.6878T>G	NP_476508.2:p.Phe2293Cys