Canonical Allele Identifier: CA351202618

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238253166A>T (hg19) ; chr2:g.237344523A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344523A>T , CM000664.2:g.237344523A>T	GRCh38
NC_000002.11:g.238253166A>T , CM000664.1:g.238253166A>T	GRCh37
NC_000002.10:g.237917905A>T	NCBI36
NG_008676.1:g.74685T>A , LRG_473:g.74685T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.140T>A
ENST00000353578.9:c.6877T>A	ENSP00000315873.4:p.Phe2293Ile
ENST00000295550.9:c.7495T>A MANE Select	ENSP00000295550.4:p.Phe2499Ile
ENST00000295550.8:c.7495T>A	ENSP00000295550.4:p.Phe2499Ile
ENST00000347401.7:c.5671T>A	ENSP00000315609.4:p.Phe1891Ile
ENST00000353578.8:c.6877T>A	ENSP00000315873.4:p.Phe2293Ile
ENST00000409809.5:c.6877T>A	ENSP00000386844.1:p.Phe2293Ile
ENST00000472056.5:c.5674T>A	ENSP00000418285.1:p.Phe1892Ile
ENST00000491769.1:n.1749T>A
NM_004369.3:c.7495T>A , LRG_473t1:c.7495T>A	NP_004360.2:p.Phe2499Ile
NM_057166.4:c.5674T>A	NP_476507.3:p.Phe1892Ile
NM_057167.3:c.6877T>A	NP_476508.2:p.Phe2293Ile
XM_005246065.1:c.6895T>A	XP_005246122.1:p.Phe2299Ile
XM_005246066.1:c.6274T>A	XP_005246123.1:p.Phe2092Ile
XM_006712253.1:c.6994T>A	XP_006712316.1:p.Phe2332Ile
XM_011510574.1:c.7492T>A	XP_011508876.1:p.Phe2498Ile
XM_011510575.1:c.5089T>A	XP_011508877.1:p.Phe1697Ile
XM_017003304.1:c.5089T>A	XP_016858793.1:p.Phe1697Ile
XM_024452684.1:c.6274T>A	XP_024308452.1:p.Phe2092Ile
NM_004369.4:c.7495T>A MANE Select	NP_004360.2:p.Phe2499Ile
NM_057166.5:c.5674T>A	NP_476507.3:p.Phe1892Ile
NM_057167.4:c.6877T>A	NP_476508.2:p.Phe2293Ile