Canonical Allele Identifier: CA1337610835

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344358C= , CM000664.2:g.237344358C=	GRCh38
NC_000002.11:g.238253001C= , CM000664.1:g.238253001C=	GRCh37
NC_000002.10:g.237917740C=	NCBI36
NG_008676.1:g.74850G= , LRG_473:g.74850G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.7660G= MANE Select	NP_004360.2:p.Ala2554=
ENST00000295550.9:c.7660G= MANE Select	ENSP00000295550.4:p.Ala2554=
NM_004369.3:c.7660G= , LRG_473t1:c.7660G=	NP_004360.2:p.Ala2554=
NM_057166.4:c.5839G=	NP_476507.3:p.Ala1947=
NM_057166.5:c.5839G=	NP_476507.3:p.Ala1947=
NM_057167.3:c.7042G=	NP_476508.2:p.Ala2348=
NM_057167.4:c.7042G=	NP_476508.2:p.Ala2348=
ENST00000295550.8:c.7660G=	ENSP00000295550.4:p.Ala2554=
ENST00000347401.7:c.5836G=	ENSP00000315609.4:p.Ala1946=
ENST00000347401.8:c.305G=
ENST00000353578.8:c.7042G=	ENSP00000315873.4:p.Ala2348=
ENST00000353578.9:c.7042G=	ENSP00000315873.4:p.Ala2348=
ENST00000409809.5:c.7042G=	ENSP00000386844.1:p.Ala2348=
ENST00000472056.5:c.5839G=	ENSP00000418285.1:p.Ala1947=
ENST00000491769.1:n.1914G=
XM_005246065.1:c.7060G=	XP_005246122.1:p.Ala2354=
XM_005246066.1:c.6439G=	XP_005246123.1:p.Ala2147=
XM_006712253.1:c.7159G=	XP_006712316.1:p.Ala2387=
XM_011510574.1:c.7657G=	XP_011508876.1:p.Ala2553=
XM_011510575.1:c.5254G=	XP_011508877.1:p.Ala1752=
XM_017003304.1:c.5254G=	XP_016858793.1:p.Ala1752=
XM_024452684.1:c.6439G=	XP_024308452.1:p.Ala2147=