Canonical Allele Identifier: CA351190884

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244786T>G (hg19) ; chr2:g.237336143T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336143T>G , CM000664.2:g.237336143T>G	GRCh38
NC_000002.11:g.238244786T>G , CM000664.1:g.238244786T>G	GRCh37
NC_000002.10:g.237909525T>G	NCBI36
NG_008676.1:g.83065A>C , LRG_473:g.83065A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1602A>C
ENST00000353578.9:c.8339A>C	ENSP00000315873.4:p.Lys2780Thr
ENST00000682957.1:c.1084A>C
ENST00000684508.1:n.1224A>C
ENST00000295550.9:c.8957A>C MANE Select	ENSP00000295550.4:p.Lys2986Thr
ENST00000295550.8:c.8957A>C	ENSP00000295550.4:p.Lys2986Thr
ENST00000347401.7:c.7133A>C	ENSP00000315609.4:p.Lys2378Thr
ENST00000353578.8:c.8339A>C	ENSP00000315873.4:p.Lys2780Thr
ENST00000409809.5:c.8339A>C	ENSP00000386844.1:p.Lys2780Thr
ENST00000472056.5:c.7136A>C	ENSP00000418285.1:p.Lys2379Thr
ENST00000491769.1:n.5399A>C
NM_004369.3:c.8957A>C , LRG_473t1:c.8957A>C	NP_004360.2:p.Lys2986Thr
NM_057166.4:c.7136A>C	NP_476507.3:p.Lys2379Thr
NM_057167.3:c.8339A>C	NP_476508.2:p.Lys2780Thr
XM_005246065.1:c.8357A>C	XP_005246122.1:p.Lys2786Thr
XM_005246066.1:c.7736A>C	XP_005246123.1:p.Lys2579Thr
XM_006712253.1:c.8456A>C	XP_006712316.1:p.Lys2819Thr
XM_011510574.1:c.8954A>C	XP_011508876.1:p.Lys2985Thr
XM_011510575.1:c.6551A>C	XP_011508877.1:p.Lys2184Thr
XM_017003304.1:c.6551A>C	XP_016858793.1:p.Lys2184Thr
XM_024452684.1:c.7736A>C	XP_024308452.1:p.Lys2579Thr
NM_004369.4:c.8957A>C MANE Select	NP_004360.2:p.Lys2986Thr
NM_057166.5:c.7136A>C	NP_476507.3:p.Lys2379Thr
NM_057167.4:c.8339A>C	NP_476508.2:p.Lys2780Thr