Canonical Allele Identifier: CA1337608619

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237340562G= , CM000664.2:g.237340562G=	GRCh38
NC_000002.11:g.238249205G= , CM000664.1:g.238249205G=	GRCh37
NC_000002.10:g.237913944G=	NCBI36
NG_008676.1:g.78646C= , LRG_473:g.78646C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.999C=
ENST00000353578.9:c.7736C=	ENSP00000315873.4:p.Thr2579=
ENST00000682957.1:c.357C=
ENST00000684508.1:n.621C=
ENST00000295550.9:c.8354C= MANE Select	ENSP00000295550.4:p.Thr2785=
ENST00000295550.8:c.8354C=	ENSP00000295550.4:p.Thr2785=
ENST00000347401.7:c.6530C=	ENSP00000315609.4:p.Thr2177=
ENST00000353578.8:c.7736C=	ENSP00000315873.4:p.Thr2579=
ENST00000409809.5:c.7736C=	ENSP00000386844.1:p.Thr2579=
ENST00000468792.1:n.41C=
ENST00000472056.5:c.6533C=	ENSP00000418285.1:p.Thr2178=
ENST00000491769.1:n.4796C=
NM_004369.3:c.8354C= , LRG_473t1:c.8354C=	NP_004360.2:p.Thr2785=
NM_057166.4:c.6533C=	NP_476507.3:p.Thr2178=
NM_057167.3:c.7736C=	NP_476508.2:p.Thr2579=
XM_005246065.1:c.7754C=	XP_005246122.1:p.Thr2585=
XM_005246066.1:c.7133C=	XP_005246123.1:p.Thr2378=
XM_006712253.1:c.7853C=	XP_006712316.1:p.Thr2618=
XM_011510574.1:c.8351C=	XP_011508876.1:p.Thr2784=
XM_011510575.1:c.5948C=	XP_011508877.1:p.Thr1983=
XM_017003304.1:c.5948C=	XP_016858793.1:p.Thr1983=
XM_024452684.1:c.7133C=	XP_024308452.1:p.Thr2378=
NM_004369.4:c.8354C= MANE Select	NP_004360.2:p.Thr2785=
NM_057166.5:c.6533C=	NP_476507.3:p.Thr2178=
NM_057167.4:c.7736C=	NP_476508.2:p.Thr2579=