Canonical Allele Identifier: CA2189782
Gene: COL6A3 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237388134del , CM000664.2:g.237388134del GRCh38
NC_000002.11:g.238296777del , CM000664.1:g.238296777del GRCh37
NC_000002.10:g.237961516del NCBI36
NG_008676.1:g.31075del , LRG_473:g.31075del

Transcript Alleles

HGVS Amino-acid Change
ENST00000353578.9:c.143del ENSP00000315873.4:p.Gly48GlufsTer13
ENST00000682405.1:n.86-6634del
ENST00000295550.9:c.761del MANE Select ENSP00000295550.4:p.Gly254GlufsTer13
ENST00000295550.8:c.761del ENSP00000295550.4:p.Gly254GlufsTer13
ENST00000347401.7:c.92-6634del ENSP00000315609.4:n.92-6634del
ENST00000353578.8:c.143del ENSP00000315873.4:p.Gly48GlufsTer13
ENST00000392003.6:c.92-6634del ENSP00000375860.2:n.92-6634del
ENST00000392004.7:c.143del ENSP00000375861.3:p.Gly48GlufsTer13
ENST00000409809.5:c.143del ENSP00000386844.1:p.Gly48GlufsTer13
ENST00000433762.1:c.761del ENSP00000389539.1:p.Gly254GlufsTer13
ENST00000472056.5:c.92-6634del ENSP00000418285.1:n.92-6634del
NM_004369.3:c.761del , LRG_473t1:c.761del NP_004360.2:p.Gly254GlufsTer13
NM_057164.4:c.92-6634del NP_476505.3:n.92-6634del
NM_057165.4:c.143del NP_476506.3:p.Gly48GlufsTer13
NM_057166.4:c.92-6634del NP_476507.3:n.92-6634del
NM_057167.3:c.143del NP_476508.2:p.Gly48GlufsTer13
XM_005246065.1:c.761del XP_005246122.1:p.Gly254GlufsTer13
XM_005246066.1:c.92-6634del XP_005246123.1:n.92-6634del
XM_006712253.1:c.761del XP_006712316.1:p.Gly254GlufsTer13
XM_011510574.1:c.761del XP_011508876.1:p.Gly254GlufsTer13
XM_011510575.1:c.91+8594del XP_011508877.1:n.91+8594del
XM_017003304.1:c.91+8594del XP_016858793.1:n.91+8594del
XM_024452684.1:c.92-6634del XP_024308452.1:n.92-6634del
NM_004369.4:c.761del MANE Select NP_004360.2:p.Gly254GlufsTer13
NM_057164.5:c.92-6634del NP_476505.3:n.92-6634del
NM_057165.5:c.143del NP_476506.3:p.Gly48GlufsTer13
NM_057166.5:c.92-6634del NP_476507.3:n.92-6634del
NM_057167.4:c.143del NP_476508.2:p.Gly48GlufsTer13