Canonical Allele Identifier: CA1337610870
Gene: COL6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237344427G= , CM000664.2:g.237344427G= GRCh38
NC_000002.11:g.238253070G= , CM000664.1:g.238253070G= GRCh37
NC_000002.10:g.237917809G= NCBI36
NG_008676.1:g.74781C= , LRG_473:g.74781C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000347401.8:c.236C=
ENST00000353578.9:c.6973C= ENSP00000315873.4:p.Leu2325=
ENST00000295550.9:c.7591C= MANE Select ENSP00000295550.4:p.Leu2531=
ENST00000295550.8:c.7591C= ENSP00000295550.4:p.Leu2531=
ENST00000347401.7:c.5767C= ENSP00000315609.4:p.Leu1923=
ENST00000353578.8:c.6973C= ENSP00000315873.4:p.Leu2325=
ENST00000409809.5:c.6973C= ENSP00000386844.1:p.Leu2325=
ENST00000472056.5:c.5770C= ENSP00000418285.1:p.Leu1924=
ENST00000491769.1:n.1845C=
NM_004369.3:c.7591C= , LRG_473t1:c.7591C= NP_004360.2:p.Leu2531=
NM_057166.4:c.5770C= NP_476507.3:p.Leu1924=
NM_057167.3:c.6973C= NP_476508.2:p.Leu2325=
XM_005246065.1:c.6991C= XP_005246122.1:p.Leu2331=
XM_005246066.1:c.6370C= XP_005246123.1:p.Leu2124=
XM_006712253.1:c.7090C= XP_006712316.1:p.Leu2364=
XM_011510574.1:c.7588C= XP_011508876.1:p.Leu2530=
XM_011510575.1:c.5185C= XP_011508877.1:p.Leu1729=
XM_017003304.1:c.5185C= XP_016858793.1:p.Leu1729=
XM_024452684.1:c.6370C= XP_024308452.1:p.Leu2124=
NM_004369.4:c.7591C= MANE Select NP_004360.2:p.Leu2531=
NM_057166.5:c.5770C= NP_476507.3:p.Leu1924=
NM_057167.4:c.6973C= NP_476508.2:p.Leu2325=