Canonical Allele Identifier: CA2663791989
Gene: COL6A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237334895A>C , CM000664.2:g.237334895A>C GRCh38
NC_000002.11:g.238243538A>C , CM000664.1:g.238243538A>C GRCh37
NC_000002.10:g.237908277A>C NCBI36
NG_008676.1:g.84313T>G , LRG_473:g.84313T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000347401.8:c.1610+1240T>G
ENST00000353578.9:c.8348-6T>G ENSP00000315873.4:n.8348-6T>G
ENST00000682957.1:c.1093-6T>G
ENST00000295550.9:c.8966-6T>G MANE Select ENSP00000295550.4:n.8966-6T>G
ENST00000295550.8:c.8966-6T>G ENSP00000295550.4:n.8966-6T>G
ENST00000347401.7:c.7142-6T>G ENSP00000315609.4:n.7142-6T>G
ENST00000353578.8:c.8348-6T>G ENSP00000315873.4:n.8348-6T>G
ENST00000409809.5:c.8348-6T>G ENSP00000386844.1:n.8348-6T>G
ENST00000472056.5:c.7145-6T>G ENSP00000418285.1:n.7145-6T>G
ENST00000491769.1:n.5408-6T>G
NM_004369.3:c.8966-6T>G , LRG_473t1:c.8966-6T>G NP_004360.2:n.8966-6T>G
NM_057166.4:c.7145-6T>G NP_476507.3:n.7145-6T>G
NM_057167.3:c.8348-6T>G NP_476508.2:n.8348-6T>G
XM_005246065.1:c.8366-6T>G XP_005246122.1:n.8366-6T>G
XM_005246066.1:c.7745-6T>G XP_005246123.1:n.7745-6T>G
XM_006712253.1:c.8465-6T>G XP_006712316.1:n.8465-6T>G
XM_011510574.1:c.8963-6T>G XP_011508876.1:n.8963-6T>G
XM_011510575.1:c.6560-6T>G XP_011508877.1:n.6560-6T>G
XM_017003304.1:c.6560-6T>G XP_016858793.1:n.6560-6T>G
XM_024452684.1:c.7745-6T>G XP_024308452.1:n.7745-6T>G
NM_004369.4:c.8966-6T>G MANE Select NP_004360.2:n.8966-6T>G
NM_057166.5:c.7145-6T>G NP_476507.3:n.7145-6T>G
NM_057167.4:c.8348-6T>G NP_476508.2:n.8348-6T>G