Canonical Allele Identifier: CA351191933
Gene: COL6A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237336458T>C , CM000664.2:g.237336458T>C GRCh38
NC_000002.11:g.238245101T>C , CM000664.1:g.238245101T>C GRCh37
NC_000002.10:g.237909840T>C NCBI36
NG_008676.1:g.82750A>G , LRG_473:g.82750A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000347401.8:c.1287A>G
ENST00000353578.9:c.8024A>G ENSP00000315873.4:p.Lys2675Arg
ENST00000682957.1:c.769A>G
ENST00000684508.1:n.909A>G
ENST00000295550.9:c.8642A>G MANE Select ENSP00000295550.4:p.Lys2881Arg
ENST00000295550.8:c.8642A>G ENSP00000295550.4:p.Lys2881Arg
ENST00000347401.7:c.6818A>G ENSP00000315609.4:p.Lys2273Arg
ENST00000353578.8:c.8024A>G ENSP00000315873.4:p.Lys2675Arg
ENST00000409809.5:c.8024A>G ENSP00000386844.1:p.Lys2675Arg
ENST00000472056.5:c.6821A>G ENSP00000418285.1:p.Lys2274Arg
ENST00000491769.1:n.5084A>G
NM_004369.3:c.8642A>G , LRG_473t1:c.8642A>G NP_004360.2:p.Lys2881Arg
NM_057166.4:c.6821A>G NP_476507.3:p.Lys2274Arg
NM_057167.3:c.8024A>G NP_476508.2:p.Lys2675Arg
XM_005246065.1:c.8042A>G XP_005246122.1:p.Lys2681Arg
XM_005246066.1:c.7421A>G XP_005246123.1:p.Lys2474Arg
XM_006712253.1:c.8141A>G XP_006712316.1:p.Lys2714Arg
XM_011510574.1:c.8639A>G XP_011508876.1:p.Lys2880Arg
XM_011510575.1:c.6236A>G XP_011508877.1:p.Lys2079Arg
XM_017003304.1:c.6236A>G XP_016858793.1:p.Lys2079Arg
XM_024452684.1:c.7421A>G XP_024308452.1:p.Lys2474Arg
NM_004369.4:c.8642A>G MANE Select NP_004360.2:p.Lys2881Arg
NM_057166.5:c.6821A>G NP_476507.3:p.Lys2274Arg
NM_057167.4:c.8024A>G NP_476508.2:p.Lys2675Arg