Canonical Allele Identifier: CA1337607225

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336480T= , CM000664.2:g.237336480T=	GRCh38
NC_000002.11:g.238245123T= , CM000664.1:g.238245123T=	GRCh37
NC_000002.10:g.237909862T=	NCBI36
NG_008676.1:g.82728A= , LRG_473:g.82728A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1265A=
ENST00000353578.9:c.8002A=	ENSP00000315873.4:p.Thr2668=
ENST00000682957.1:c.747A=
ENST00000684508.1:n.887A=
ENST00000295550.9:c.8620A= MANE Select	ENSP00000295550.4:p.Thr2874=
ENST00000295550.8:c.8620A=	ENSP00000295550.4:p.Thr2874=
ENST00000347401.7:c.6796A=	ENSP00000315609.4:p.Thr2266=
ENST00000353578.8:c.8002A=	ENSP00000315873.4:p.Thr2668=
ENST00000409809.5:c.8002A=	ENSP00000386844.1:p.Thr2668=
ENST00000472056.5:c.6799A=	ENSP00000418285.1:p.Thr2267=
ENST00000491769.1:n.5062A=
NM_004369.3:c.8620A= , LRG_473t1:c.8620A=	NP_004360.2:p.Thr2874=
NM_057166.4:c.6799A=	NP_476507.3:p.Thr2267=
NM_057167.3:c.8002A=	NP_476508.2:p.Thr2668=
XM_005246065.1:c.8020A=	XP_005246122.1:p.Thr2674=
XM_005246066.1:c.7399A=	XP_005246123.1:p.Thr2467=
XM_006712253.1:c.8119A=	XP_006712316.1:p.Thr2707=
XM_011510574.1:c.8617A=	XP_011508876.1:p.Thr2873=
XM_011510575.1:c.6214A=	XP_011508877.1:p.Thr2072=
XM_017003304.1:c.6214A=	XP_016858793.1:p.Thr2072=
XM_024452684.1:c.7399A=	XP_024308452.1:p.Thr2467=
NM_004369.4:c.8620A= MANE Select	NP_004360.2:p.Thr2874=
NM_057166.5:c.6799A=	NP_476507.3:p.Thr2267=
NM_057167.4:c.8002A=	NP_476508.2:p.Thr2668=