Canonical Allele Identifier: CA431678315

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238267849A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237359206A>G , CM000664.2:g.237359206A>G	GRCh38
NC_000002.11:g.238267849A>G , CM000664.1:g.238267849A>G	GRCh37
NC_000002.10:g.237932588A>G	NCBI36
NG_008676.1:g.60002T>C , LRG_473:g.60002T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.5736T>C	ENSP00000315873.4:p.Asp1912=
ENST00000295550.9:c.6354T>C MANE Select	ENSP00000295550.4:p.Asp2118=
ENST00000295550.8:c.6354T>C	ENSP00000295550.4:p.Asp2118=
ENST00000347401.7:c.4533T>C	ENSP00000315609.4:p.Asp1511=
ENST00000353578.8:c.5736T>C	ENSP00000315873.4:p.Asp1912=
ENST00000409809.5:c.5736T>C	ENSP00000386844.1:p.Asp1912=
ENST00000472056.5:c.4533T>C	ENSP00000418285.1:p.Asp1511=
NM_004369.3:c.6354T>C , LRG_473t1:c.6354T>C	NP_004360.2:p.Asp2118=
NM_057166.4:c.4533T>C	NP_476507.3:p.Asp1511=
NM_057167.3:c.5736T>C	NP_476508.2:p.Asp1912=
XM_005246065.1:c.5754T>C	XP_005246122.1:p.Asp1918=
XM_005246066.1:c.5133T>C	XP_005246123.1:p.Asp1711=
XM_006712253.1:c.5853T>C	XP_006712316.1:p.Asp1951=
XM_011510574.1:c.6351T>C	XP_011508876.1:p.Asp2117=
XM_011510575.1:c.3948T>C	XP_011508877.1:p.Asp1316=
XM_017003304.1:c.3948T>C	XP_016858793.1:p.Asp1316=
XM_024452684.1:c.5133T>C	XP_024308452.1:p.Asp1711=
NM_004369.4:c.6354T>C MANE Select	NP_004360.2:p.Asp2118=
NM_057166.5:c.4533T>C	NP_476507.3:p.Asp1511=
NM_057167.4:c.5736T>C	NP_476508.2:p.Asp1912=