Canonical Allele Identifier: CA1337607236

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336512G= , CM000664.2:g.237336512G=	GRCh38
NC_000002.11:g.238245155G= , CM000664.1:g.238245155G=	GRCh37
NC_000002.10:g.237909894G=	NCBI36
NG_008676.1:g.82696C= , LRG_473:g.82696C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1233C=
ENST00000353578.9:c.7970C=	ENSP00000315873.4:p.Thr2657=
ENST00000682957.1:c.715C=
ENST00000684508.1:n.855C=
ENST00000295550.9:c.8588C= MANE Select	ENSP00000295550.4:p.Thr2863=
ENST00000295550.8:c.8588C=	ENSP00000295550.4:p.Thr2863=
ENST00000347401.7:c.6764C=	ENSP00000315609.4:p.Thr2255=
ENST00000353578.8:c.7970C=	ENSP00000315873.4:p.Thr2657=
ENST00000409809.5:c.7970C=	ENSP00000386844.1:p.Thr2657=
ENST00000472056.5:c.6767C=	ENSP00000418285.1:p.Thr2256=
ENST00000491769.1:n.5030C=
NM_004369.3:c.8588C= , LRG_473t1:c.8588C=	NP_004360.2:p.Thr2863=
NM_057166.4:c.6767C=	NP_476507.3:p.Thr2256=
NM_057167.3:c.7970C=	NP_476508.2:p.Thr2657=
XM_005246065.1:c.7988C=	XP_005246122.1:p.Thr2663=
XM_005246066.1:c.7367C=	XP_005246123.1:p.Thr2456=
XM_006712253.1:c.8087C=	XP_006712316.1:p.Thr2696=
XM_011510574.1:c.8585C=	XP_011508876.1:p.Thr2862=
XM_011510575.1:c.6182C=	XP_011508877.1:p.Thr2061=
XM_017003304.1:c.6182C=	XP_016858793.1:p.Thr2061=
XM_024452684.1:c.7367C=	XP_024308452.1:p.Thr2456=
NM_004369.4:c.8588C= MANE Select	NP_004360.2:p.Thr2863=
NM_057166.5:c.6767C=	NP_476507.3:p.Thr2256=
NM_057167.4:c.7970C=	NP_476508.2:p.Thr2657=