Canonical Allele Identifier: CA351191867
Gene: COL6A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237336423T>G , CM000664.2:g.237336423T>G GRCh38
NC_000002.11:g.238245066T>G , CM000664.1:g.238245066T>G GRCh37
NC_000002.10:g.237909805T>G NCBI36
NG_008676.1:g.82785A>C , LRG_473:g.82785A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000347401.8:c.1322A>C
ENST00000353578.9:c.8059A>C ENSP00000315873.4:p.Thr2687Pro
ENST00000682957.1:c.804A>C
ENST00000684508.1:n.944A>C
ENST00000295550.9:c.8677A>C MANE Select ENSP00000295550.4:p.Thr2893Pro
ENST00000295550.8:c.8677A>C ENSP00000295550.4:p.Thr2893Pro
ENST00000347401.7:c.6853A>C ENSP00000315609.4:p.Thr2285Pro
ENST00000353578.8:c.8059A>C ENSP00000315873.4:p.Thr2687Pro
ENST00000409809.5:c.8059A>C ENSP00000386844.1:p.Thr2687Pro
ENST00000472056.5:c.6856A>C ENSP00000418285.1:p.Thr2286Pro
ENST00000491769.1:n.5119A>C
NM_004369.3:c.8677A>C , LRG_473t1:c.8677A>C NP_004360.2:p.Thr2893Pro
NM_057166.4:c.6856A>C NP_476507.3:p.Thr2286Pro
NM_057167.3:c.8059A>C NP_476508.2:p.Thr2687Pro
XM_005246065.1:c.8077A>C XP_005246122.1:p.Thr2693Pro
XM_005246066.1:c.7456A>C XP_005246123.1:p.Thr2486Pro
XM_006712253.1:c.8176A>C XP_006712316.1:p.Thr2726Pro
XM_011510574.1:c.8674A>C XP_011508876.1:p.Thr2892Pro
XM_011510575.1:c.6271A>C XP_011508877.1:p.Thr2091Pro
XM_017003304.1:c.6271A>C XP_016858793.1:p.Thr2091Pro
XM_024452684.1:c.7456A>C XP_024308452.1:p.Thr2486Pro
NM_004369.4:c.8677A>C MANE Select NP_004360.2:p.Thr2893Pro
NM_057166.5:c.6856A>C NP_476507.3:p.Thr2286Pro
NM_057167.4:c.8059A>C NP_476508.2:p.Thr2687Pro