Canonical Allele Identifier: CA431699145

Gene: COL6A3

Linked Data

• COSMIC: COSM1178115
• MyVariant Identifiers: chr2:g.238243429G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237334786G>T , CM000664.2:g.237334786G>T	GRCh38
NC_000002.11:g.238243429G>T , CM000664.1:g.238243429G>T	GRCh37
NC_000002.10:g.237908168G>T	NCBI36
NG_008676.1:g.84422C>A , LRG_473:g.84422C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000347401.8:c.1611-1238C>A
ENST00000353578.9:c.8451C>A	ENSP00000315873.4:p.Thr2817=
ENST00000682957.1:c.1196C>A
ENST00000295550.9:c.9069C>A MANE Select	ENSP00000295550.4:p.Thr3023=
ENST00000295550.8:c.9069C>A	ENSP00000295550.4:p.Thr3023=
ENST00000347401.7:c.7245C>A	ENSP00000315609.4:p.Thr2415=
ENST00000353578.8:c.8451C>A	ENSP00000315873.4:p.Thr2817=
ENST00000409809.5:c.8451C>A	ENSP00000386844.1:p.Thr2817=
ENST00000472056.5:c.7248C>A	ENSP00000418285.1:p.Thr2416=
ENST00000491769.1:n.5511C>A
ENST00000493608.1:n.1C>A
NM_004369.3:c.9069C>A , LRG_473t1:c.9069C>A	NP_004360.2:p.Thr3023=
NM_057166.4:c.7248C>A	NP_476507.3:p.Thr2416=
NM_057167.3:c.8451C>A	NP_476508.2:p.Thr2817=
XM_005246065.1:c.8469C>A	XP_005246122.1:p.Thr2823=
XM_005246066.1:c.7848C>A	XP_005246123.1:p.Thr2616=
XM_006712253.1:c.8568C>A	XP_006712316.1:p.Thr2856=
XM_011510574.1:c.9066C>A	XP_011508876.1:p.Thr3022=
XM_011510575.1:c.6663C>A	XP_011508877.1:p.Thr2221=
XM_017003304.1:c.6663C>A	XP_016858793.1:p.Thr2221=
XM_024452684.1:c.7848C>A	XP_024308452.1:p.Thr2616=
NM_004369.4:c.9069C>A MANE Select	NP_004360.2:p.Thr3023=
NM_057166.5:c.7248C>A	NP_476507.3:p.Thr2416=
NM_057167.4:c.8451C>A	NP_476508.2:p.Thr2817=