Canonical Allele Identifier: CA351192006
Gene: COL6A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237336497G>T , CM000664.2:g.237336497G>T GRCh38
NC_000002.11:g.238245140G>T , CM000664.1:g.238245140G>T GRCh37
NC_000002.10:g.237909879G>T NCBI36
NG_008676.1:g.82711C>A , LRG_473:g.82711C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000347401.8:c.1248C>A
ENST00000353578.9:c.7985C>A ENSP00000315873.4:p.Ser2662Tyr
ENST00000682957.1:c.730C>A
ENST00000684508.1:n.870C>A
ENST00000295550.9:c.8603C>A MANE Select ENSP00000295550.4:p.Ser2868Tyr
ENST00000295550.8:c.8603C>A ENSP00000295550.4:p.Ser2868Tyr
ENST00000347401.7:c.6779C>A ENSP00000315609.4:p.Ser2260Tyr
ENST00000353578.8:c.7985C>A ENSP00000315873.4:p.Ser2662Tyr
ENST00000409809.5:c.7985C>A ENSP00000386844.1:p.Ser2662Tyr
ENST00000472056.5:c.6782C>A ENSP00000418285.1:p.Ser2261Tyr
ENST00000491769.1:n.5045C>A
NM_004369.3:c.8603C>A , LRG_473t1:c.8603C>A NP_004360.2:p.Ser2868Tyr
NM_057166.4:c.6782C>A NP_476507.3:p.Ser2261Tyr
NM_057167.3:c.7985C>A NP_476508.2:p.Ser2662Tyr
XM_005246065.1:c.8003C>A XP_005246122.1:p.Ser2668Tyr
XM_005246066.1:c.7382C>A XP_005246123.1:p.Ser2461Tyr
XM_006712253.1:c.8102C>A XP_006712316.1:p.Ser2701Tyr
XM_011510574.1:c.8600C>A XP_011508876.1:p.Ser2867Tyr
XM_011510575.1:c.6197C>A XP_011508877.1:p.Ser2066Tyr
XM_017003304.1:c.6197C>A XP_016858793.1:p.Ser2066Tyr
XM_024452684.1:c.7382C>A XP_024308452.1:p.Ser2461Tyr
NM_004369.4:c.8603C>A MANE Select NP_004360.2:p.Ser2868Tyr
NM_057166.5:c.6782C>A NP_476507.3:p.Ser2261Tyr
NM_057167.4:c.7985C>A NP_476508.2:p.Ser2662Tyr