Canonical Allele Identifier: CA351188796
Gene: COL6A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237334790A>G , CM000664.2:g.237334790A>G GRCh38
NC_000002.11:g.238243433A>G , CM000664.1:g.238243433A>G GRCh37
NC_000002.10:g.237908172A>G NCBI36
NG_008676.1:g.84418T>C , LRG_473:g.84418T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000347401.8:c.1611-1242T>C
ENST00000353578.9:c.8447T>C ENSP00000315873.4:p.Leu2816Pro
ENST00000682957.1:c.1192T>C
ENST00000295550.9:c.9065T>C MANE Select ENSP00000295550.4:p.Leu3022Pro
ENST00000295550.8:c.9065T>C ENSP00000295550.4:p.Leu3022Pro
ENST00000347401.7:c.7241T>C ENSP00000315609.4:p.Leu2414Pro
ENST00000353578.8:c.8447T>C ENSP00000315873.4:p.Leu2816Pro
ENST00000409809.5:c.8447T>C ENSP00000386844.1:p.Leu2816Pro
ENST00000472056.5:c.7244T>C ENSP00000418285.1:p.Leu2415Pro
ENST00000491769.1:n.5507T>C
NM_004369.3:c.9065T>C , LRG_473t1:c.9065T>C NP_004360.2:p.Leu3022Pro
NM_057166.4:c.7244T>C NP_476507.3:p.Leu2415Pro
NM_057167.3:c.8447T>C NP_476508.2:p.Leu2816Pro
XM_005246065.1:c.8465T>C XP_005246122.1:p.Leu2822Pro
XM_005246066.1:c.7844T>C XP_005246123.1:p.Leu2615Pro
XM_006712253.1:c.8564T>C XP_006712316.1:p.Leu2855Pro
XM_011510574.1:c.9062T>C XP_011508876.1:p.Leu3021Pro
XM_011510575.1:c.6659T>C XP_011508877.1:p.Leu2220Pro
XM_017003304.1:c.6659T>C XP_016858793.1:p.Leu2220Pro
XM_024452684.1:c.7844T>C XP_024308452.1:p.Leu2615Pro
NM_004369.4:c.9065T>C MANE Select NP_004360.2:p.Leu3022Pro
NM_057166.5:c.7244T>C NP_476507.3:p.Leu2415Pro
NM_057167.4:c.8447T>C NP_476508.2:p.Leu2816Pro