Canonical Allele Identifier: CA431702509

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238245082T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336439T>C , CM000664.2:g.237336439T>C	GRCh38
NC_000002.11:g.238245082T>C , CM000664.1:g.238245082T>C	GRCh37
NC_000002.10:g.237909821T>C	NCBI36
NG_008676.1:g.82769A>G , LRG_473:g.82769A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1306A>G
ENST00000353578.9:c.8043A>G	ENSP00000315873.4:p.Thr2681=
ENST00000682957.1:c.788A>G
ENST00000684508.1:n.928A>G
ENST00000295550.9:c.8661A>G MANE Select	ENSP00000295550.4:p.Thr2887=
ENST00000295550.8:c.8661A>G	ENSP00000295550.4:p.Thr2887=
ENST00000347401.7:c.6837A>G	ENSP00000315609.4:p.Thr2279=
ENST00000353578.8:c.8043A>G	ENSP00000315873.4:p.Thr2681=
ENST00000409809.5:c.8043A>G	ENSP00000386844.1:p.Thr2681=
ENST00000472056.5:c.6840A>G	ENSP00000418285.1:p.Thr2280=
ENST00000491769.1:n.5103A>G
NM_004369.3:c.8661A>G , LRG_473t1:c.8661A>G	NP_004360.2:p.Thr2887=
NM_057166.4:c.6840A>G	NP_476507.3:p.Thr2280=
NM_057167.3:c.8043A>G	NP_476508.2:p.Thr2681=
XM_005246065.1:c.8061A>G	XP_005246122.1:p.Thr2687=
XM_005246066.1:c.7440A>G	XP_005246123.1:p.Thr2480=
XM_006712253.1:c.8160A>G	XP_006712316.1:p.Thr2720=
XM_011510574.1:c.8658A>G	XP_011508876.1:p.Thr2886=
XM_011510575.1:c.6255A>G	XP_011508877.1:p.Thr2085=
XM_017003304.1:c.6255A>G	XP_016858793.1:p.Thr2085=
XM_024452684.1:c.7440A>G	XP_024308452.1:p.Thr2480=
NM_004369.4:c.8661A>G MANE Select	NP_004360.2:p.Thr2887=
NM_057166.5:c.6840A>G	NP_476507.3:p.Thr2280=
NM_057167.4:c.8043A>G	NP_476508.2:p.Thr2681=