Canonical Allele Identifier: CA2189121
Gene: COL6A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 425260
dbSNP Id: rs772944531

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237374423A>G , CM000664.2:g.237374423A>G GRCh38
NC_000002.11:g.238283066A>G , CM000664.1:g.238283066A>G GRCh37
NC_000002.10:g.237947805A>G NCBI36
NG_008676.1:g.44785T>C , LRG_473:g.44785T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000353578.9:c.3050T>C ENSP00000315873.4:p.Leu1017Pro
ENST00000295550.9:c.3668T>C MANE Select ENSP00000295550.4:p.Leu1223Pro
ENST00000295550.8:c.3668T>C ENSP00000295550.4:p.Leu1223Pro
ENST00000347401.7:c.1847T>C ENSP00000315609.4:p.Leu616Pro
ENST00000353578.8:c.3050T>C ENSP00000315873.4:p.Leu1017Pro
ENST00000392003.6:c.2447T>C ENSP00000375860.2:p.Leu816Pro
ENST00000392004.7:c.3050T>C ENSP00000375861.3:p.Leu1017Pro
ENST00000409809.5:c.3050T>C ENSP00000386844.1:p.Leu1017Pro
ENST00000472056.5:c.1847T>C ENSP00000418285.1:p.Leu616Pro
NM_004369.3:c.3668T>C , LRG_473t1:c.3668T>C NP_004360.2:p.Leu1223Pro
NM_057164.4:c.2447T>C NP_476505.3:p.Leu816Pro
NM_057165.4:c.3050T>C NP_476506.3:p.Leu1017Pro
NM_057166.4:c.1847T>C NP_476507.3:p.Leu616Pro
NM_057167.3:c.3050T>C NP_476508.2:p.Leu1017Pro
XM_005246065.1:c.3068T>C XP_005246122.1:p.Leu1023Pro
XM_005246066.1:c.2447T>C XP_005246123.1:p.Leu816Pro
XM_006712253.1:c.3668T>C XP_006712316.1:p.Leu1223Pro
XM_011510574.1:c.3668T>C XP_011508876.1:p.Leu1223Pro
XM_011510575.1:c.1262T>C XP_011508877.1:p.Leu421Pro
XM_017003304.1:c.1262T>C XP_016858793.1:p.Leu421Pro
XM_024452684.1:c.2447T>C XP_024308452.1:p.Leu816Pro
NM_004369.4:c.3668T>C MANE Select NP_004360.2:p.Leu1223Pro
NM_057164.5:c.2447T>C NP_476505.3:p.Leu816Pro
NM_057165.5:c.3050T>C NP_476506.3:p.Leu1017Pro
NM_057166.5:c.1847T>C NP_476507.3:p.Leu616Pro
NM_057167.4:c.3050T>C NP_476508.2:p.Leu1017Pro