Canonical Allele Identifier: CA351202003

Gene: COL6A3

Linked Data

• COSMIC: COSM3051280
• MyVariant Identifiers: chr2:g.238253080T>G (hg19) ; chr2:g.237344437T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344437T>G , CM000664.2:g.237344437T>G	GRCh38
NC_000002.11:g.238253080T>G , CM000664.1:g.238253080T>G	GRCh37
NC_000002.10:g.237917819T>G	NCBI36
NG_008676.1:g.74771A>C , LRG_473:g.74771A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.226A>C
ENST00000353578.9:c.6963A>C	ENSP00000315873.4:p.Arg2321Ser
ENST00000295550.9:c.7581A>C MANE Select	ENSP00000295550.4:p.Arg2527Ser
ENST00000295550.8:c.7581A>C	ENSP00000295550.4:p.Arg2527Ser
ENST00000347401.7:c.5757A>C	ENSP00000315609.4:p.Arg1919Ser
ENST00000353578.8:c.6963A>C	ENSP00000315873.4:p.Arg2321Ser
ENST00000409809.5:c.6963A>C	ENSP00000386844.1:p.Arg2321Ser
ENST00000472056.5:c.5760A>C	ENSP00000418285.1:p.Arg1920Ser
ENST00000491769.1:n.1835A>C
NM_004369.3:c.7581A>C , LRG_473t1:c.7581A>C	NP_004360.2:p.Arg2527Ser
NM_057166.4:c.5760A>C	NP_476507.3:p.Arg1920Ser
NM_057167.3:c.6963A>C	NP_476508.2:p.Arg2321Ser
XM_005246065.1:c.6981A>C	XP_005246122.1:p.Arg2327Ser
XM_005246066.1:c.6360A>C	XP_005246123.1:p.Arg2120Ser
XM_006712253.1:c.7080A>C	XP_006712316.1:p.Arg2360Ser
XM_011510574.1:c.7578A>C	XP_011508876.1:p.Arg2526Ser
XM_011510575.1:c.5175A>C	XP_011508877.1:p.Arg1725Ser
XM_017003304.1:c.5175A>C	XP_016858793.1:p.Arg1725Ser
XM_024452684.1:c.6360A>C	XP_024308452.1:p.Arg2120Ser
NM_004369.4:c.7581A>C MANE Select	NP_004360.2:p.Arg2527Ser
NM_057166.5:c.5760A>C	NP_476507.3:p.Arg1920Ser
NM_057167.4:c.6963A>C	NP_476508.2:p.Arg2321Ser