Canonical Allele Identifier: CA351191969
Gene: COL6A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237336477T>G , CM000664.2:g.237336477T>G GRCh38
NC_000002.11:g.238245120T>G , CM000664.1:g.238245120T>G GRCh37
NC_000002.10:g.237909859T>G NCBI36
NG_008676.1:g.82731A>C , LRG_473:g.82731A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000347401.8:c.1268A>C
ENST00000353578.9:c.8005A>C ENSP00000315873.4:p.Lys2669Gln
ENST00000682957.1:c.750A>C
ENST00000684508.1:n.890A>C
ENST00000295550.9:c.8623A>C MANE Select ENSP00000295550.4:p.Lys2875Gln
ENST00000295550.8:c.8623A>C ENSP00000295550.4:p.Lys2875Gln
ENST00000347401.7:c.6799A>C ENSP00000315609.4:p.Lys2267Gln
ENST00000353578.8:c.8005A>C ENSP00000315873.4:p.Lys2669Gln
ENST00000409809.5:c.8005A>C ENSP00000386844.1:p.Lys2669Gln
ENST00000472056.5:c.6802A>C ENSP00000418285.1:p.Lys2268Gln
ENST00000491769.1:n.5065A>C
NM_004369.3:c.8623A>C , LRG_473t1:c.8623A>C NP_004360.2:p.Lys2875Gln
NM_057166.4:c.6802A>C NP_476507.3:p.Lys2268Gln
NM_057167.3:c.8005A>C NP_476508.2:p.Lys2669Gln
XM_005246065.1:c.8023A>C XP_005246122.1:p.Lys2675Gln
XM_005246066.1:c.7402A>C XP_005246123.1:p.Lys2468Gln
XM_006712253.1:c.8122A>C XP_006712316.1:p.Lys2708Gln
XM_011510574.1:c.8620A>C XP_011508876.1:p.Lys2874Gln
XM_011510575.1:c.6217A>C XP_011508877.1:p.Lys2073Gln
XM_017003304.1:c.6217A>C XP_016858793.1:p.Lys2073Gln
XM_024452684.1:c.7402A>C XP_024308452.1:p.Lys2468Gln
NM_004369.4:c.8623A>C MANE Select NP_004360.2:p.Lys2875Gln
NM_057166.5:c.6802A>C NP_476507.3:p.Lys2268Gln
NM_057167.4:c.8005A>C NP_476508.2:p.Lys2669Gln