Canonical Allele Identifier: CA2189456
Gene: COL6A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 476508
dbSNP Id: rs150008830

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237378927C>T , CM000664.2:g.237378927C>T GRCh38
NC_000002.11:g.238287570C>T , CM000664.1:g.238287570C>T GRCh37
NC_000002.10:g.237952309C>T NCBI36
NG_008676.1:g.40281G>A , LRG_473:g.40281G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000353578.9:c.1588G>A ENSP00000315873.4:p.Gly530Ser
ENST00000295550.9:c.2206G>A MANE Select ENSP00000295550.4:p.Gly736Ser
ENST00000295550.8:c.2206G>A ENSP00000295550.4:p.Gly736Ser
ENST00000347401.7:c.677-1583G>A ENSP00000315609.4:n.677-1583G>A
ENST00000353578.8:c.1588G>A ENSP00000315873.4:p.Gly530Ser
ENST00000392003.6:c.985G>A ENSP00000375860.2:p.Gly329Ser
ENST00000392004.7:c.1588G>A ENSP00000375861.3:p.Gly530Ser
ENST00000409809.5:c.1588G>A ENSP00000386844.1:p.Gly530Ser
ENST00000433762.1:c.1898-1583G>A ENSP00000389539.1:n.1898-1583G>A
ENST00000472056.5:c.677-1583G>A ENSP00000418285.1:n.677-1583G>A
NM_004369.3:c.2206G>A , LRG_473t1:c.2206G>A NP_004360.2:p.Gly736Ser
NM_057164.4:c.985G>A NP_476505.3:p.Gly329Ser
NM_057165.4:c.1588G>A NP_476506.3:p.Gly530Ser
NM_057166.4:c.677-1583G>A NP_476507.3:n.677-1583G>A
NM_057167.3:c.1588G>A NP_476508.2:p.Gly530Ser
XM_005246065.1:c.1898-1583G>A XP_005246122.1:n.1898-1583G>A
XM_005246066.1:c.985G>A XP_005246123.1:p.Gly329Ser
XM_006712253.1:c.2206G>A XP_006712316.1:p.Gly736Ser
XM_011510574.1:c.2206G>A XP_011508876.1:p.Gly736Ser
XM_011510575.1:c.92-1583G>A XP_011508877.1:n.92-1583G>A
XM_017003304.1:c.92-1583G>A XP_016858793.1:n.92-1583G>A
XM_024452684.1:c.985G>A XP_024308452.1:p.Gly329Ser
NM_004369.4:c.2206G>A MANE Select NP_004360.2:p.Gly736Ser
NM_057164.5:c.985G>A NP_476505.3:p.Gly329Ser
NM_057165.5:c.1588G>A NP_476506.3:p.Gly530Ser
NM_057166.5:c.677-1583G>A NP_476507.3:n.677-1583G>A
NM_057167.4:c.1588G>A NP_476508.2:p.Gly530Ser