Canonical Allele Identifier: CA1337606504

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237334888A= , CM000664.2:g.237334888A=	GRCh38
NC_000002.11:g.238243531A= , CM000664.1:g.238243531A=	GRCh37
NC_000002.10:g.237908270A=	NCBI36
NG_008676.1:g.84320T= , LRG_473:g.84320T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000347401.8:c.1610+1247T=
ENST00000353578.9:c.8349T=	ENSP00000315873.4:p.Val2783=
ENST00000682957.1:c.1094T=
ENST00000295550.9:c.8967T= MANE Select	ENSP00000295550.4:p.Val2989=
ENST00000295550.8:c.8967T=	ENSP00000295550.4:p.Val2989=
ENST00000347401.7:c.7143T=	ENSP00000315609.4:p.Val2381=
ENST00000353578.8:c.8349T=	ENSP00000315873.4:p.Val2783=
ENST00000409809.5:c.8349T=	ENSP00000386844.1:p.Val2783=
ENST00000472056.5:c.7146T=	ENSP00000418285.1:p.Val2382=
ENST00000491769.1:n.5409T=
NM_004369.3:c.8967T= , LRG_473t1:c.8967T=	NP_004360.2:p.Val2989=
NM_057166.4:c.7146T=	NP_476507.3:p.Val2382=
NM_057167.3:c.8349T=	NP_476508.2:p.Val2783=
XM_005246065.1:c.8367T=	XP_005246122.1:p.Val2789=
XM_005246066.1:c.7746T=	XP_005246123.1:p.Val2582=
XM_006712253.1:c.8466T=	XP_006712316.1:p.Val2822=
XM_011510574.1:c.8964T=	XP_011508876.1:p.Val2988=
XM_011510575.1:c.6561T=	XP_011508877.1:p.Val2187=
XM_017003304.1:c.6561T=	XP_016858793.1:p.Val2187=
XM_024452684.1:c.7746T=	XP_024308452.1:p.Val2582=
NM_004369.4:c.8967T= MANE Select	NP_004360.2:p.Val2989=
NM_057166.5:c.7146T=	NP_476507.3:p.Val2382=
NM_057167.4:c.8349T=	NP_476508.2:p.Val2783=