Canonical Allele Identifier: CA351202020

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238253082T>A (hg19) ; chr2:g.237344439T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344439T>A , CM000664.2:g.237344439T>A	GRCh38
NC_000002.11:g.238253082T>A , CM000664.1:g.238253082T>A	GRCh37
NC_000002.10:g.237917821T>A	NCBI36
NG_008676.1:g.74769A>T , LRG_473:g.74769A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.224A>T
ENST00000353578.9:c.6961A>T	ENSP00000315873.4:p.Arg2321Ter
ENST00000295550.9:c.7579A>T MANE Select	ENSP00000295550.4:p.Arg2527Ter
ENST00000295550.8:c.7579A>T	ENSP00000295550.4:p.Arg2527Ter
ENST00000347401.7:c.5755A>T	ENSP00000315609.4:p.Arg1919Ter
ENST00000353578.8:c.6961A>T	ENSP00000315873.4:p.Arg2321Ter
ENST00000409809.5:c.6961A>T	ENSP00000386844.1:p.Arg2321Ter
ENST00000472056.5:c.5758A>T	ENSP00000418285.1:p.Arg1920Ter
ENST00000491769.1:n.1833A>T
NM_004369.3:c.7579A>T , LRG_473t1:c.7579A>T	NP_004360.2:p.Arg2527Ter
NM_057166.4:c.5758A>T	NP_476507.3:p.Arg1920Ter
NM_057167.3:c.6961A>T	NP_476508.2:p.Arg2321Ter
XM_005246065.1:c.6979A>T	XP_005246122.1:p.Arg2327Ter
XM_005246066.1:c.6358A>T	XP_005246123.1:p.Arg2120Ter
XM_006712253.1:c.7078A>T	XP_006712316.1:p.Arg2360Ter
XM_011510574.1:c.7576A>T	XP_011508876.1:p.Arg2526Ter
XM_011510575.1:c.5173A>T	XP_011508877.1:p.Arg1725Ter
XM_017003304.1:c.5173A>T	XP_016858793.1:p.Arg1725Ter
XM_024452684.1:c.6358A>T	XP_024308452.1:p.Arg2120Ter
NM_004369.4:c.7579A>T MANE Select	NP_004360.2:p.Arg2527Ter
NM_057166.5:c.5758A>T	NP_476507.3:p.Arg1920Ter
NM_057167.4:c.6961A>T	NP_476508.2:p.Arg2321Ter