Canonical Allele Identifier: CA351202675

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238253175T>A (hg19) ; chr2:g.237344532T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344532T>A , CM000664.2:g.237344532T>A	GRCh38
NC_000002.11:g.238253175T>A , CM000664.1:g.238253175T>A	GRCh37
NC_000002.10:g.237917914T>A	NCBI36
NG_008676.1:g.74676A>T , LRG_473:g.74676A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.131A>T
ENST00000353578.9:c.6868A>T	ENSP00000315873.4:p.Arg2290Trp
ENST00000295550.9:c.7486A>T MANE Select	ENSP00000295550.4:p.Arg2496Trp
ENST00000295550.8:c.7486A>T	ENSP00000295550.4:p.Arg2496Trp
ENST00000347401.7:c.5662A>T	ENSP00000315609.4:p.Arg1888Trp
ENST00000353578.8:c.6868A>T	ENSP00000315873.4:p.Arg2290Trp
ENST00000409809.5:c.6868A>T	ENSP00000386844.1:p.Arg2290Trp
ENST00000472056.5:c.5665A>T	ENSP00000418285.1:p.Arg1889Trp
ENST00000491769.1:n.1740A>T
NM_004369.3:c.7486A>T , LRG_473t1:c.7486A>T	NP_004360.2:p.Arg2496Trp
NM_057166.4:c.5665A>T	NP_476507.3:p.Arg1889Trp
NM_057167.3:c.6868A>T	NP_476508.2:p.Arg2290Trp
XM_005246065.1:c.6886A>T	XP_005246122.1:p.Arg2296Trp
XM_005246066.1:c.6265A>T	XP_005246123.1:p.Arg2089Trp
XM_006712253.1:c.6985A>T	XP_006712316.1:p.Arg2329Trp
XM_011510574.1:c.7483A>T	XP_011508876.1:p.Arg2495Trp
XM_011510575.1:c.5080A>T	XP_011508877.1:p.Arg1694Trp
XM_017003304.1:c.5080A>T	XP_016858793.1:p.Arg1694Trp
XM_024452684.1:c.6265A>T	XP_024308452.1:p.Arg2089Trp
NM_004369.4:c.7486A>T MANE Select	NP_004360.2:p.Arg2496Trp
NM_057166.5:c.5665A>T	NP_476507.3:p.Arg1889Trp
NM_057167.4:c.6868A>T	NP_476508.2:p.Arg2290Trp