Canonical Allele Identifier: CA1337607177

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336393G= , CM000664.2:g.237336393G=	GRCh38
NC_000002.11:g.238245036G= , CM000664.1:g.238245036G=	GRCh37
NC_000002.10:g.237909775G=	NCBI36
NG_008676.1:g.82815C= , LRG_473:g.82815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1352C=
ENST00000353578.9:c.8089C=	ENSP00000315873.4:p.Pro2697=
ENST00000682957.1:c.834C=
ENST00000684508.1:n.974C=
ENST00000295550.9:c.8707C= MANE Select	ENSP00000295550.4:p.Pro2903=
ENST00000295550.8:c.8707C=	ENSP00000295550.4:p.Pro2903=
ENST00000347401.7:c.6883C=	ENSP00000315609.4:p.Pro2295=
ENST00000353578.8:c.8089C=	ENSP00000315873.4:p.Pro2697=
ENST00000409809.5:c.8089C=	ENSP00000386844.1:p.Pro2697=
ENST00000472056.5:c.6886C=	ENSP00000418285.1:p.Pro2296=
ENST00000491769.1:n.5149C=
NM_004369.3:c.8707C= , LRG_473t1:c.8707C=	NP_004360.2:p.Pro2903=
NM_057166.4:c.6886C=	NP_476507.3:p.Pro2296=
NM_057167.3:c.8089C=	NP_476508.2:p.Pro2697=
XM_005246065.1:c.8107C=	XP_005246122.1:p.Pro2703=
XM_005246066.1:c.7486C=	XP_005246123.1:p.Pro2496=
XM_006712253.1:c.8206C=	XP_006712316.1:p.Pro2736=
XM_011510574.1:c.8704C=	XP_011508876.1:p.Pro2902=
XM_011510575.1:c.6301C=	XP_011508877.1:p.Pro2101=
XM_017003304.1:c.6301C=	XP_016858793.1:p.Pro2101=
XM_024452684.1:c.7486C=	XP_024308452.1:p.Pro2496=
NM_004369.4:c.8707C= MANE Select	NP_004360.2:p.Pro2903=
NM_057166.5:c.6886C=	NP_476507.3:p.Pro2296=
NM_057167.4:c.8089C=	NP_476508.2:p.Pro2697=