Canonical Allele Identifier: CA2663795157
Gene: COL6A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237360203T>A , CM000664.2:g.237360203T>A GRCh38
NC_000002.11:g.238268846T>A , CM000664.1:g.238268846T>A GRCh37
NC_000002.10:g.237933585T>A NCBI36
NG_008676.1:g.59005A>T , LRG_473:g.59005A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000353578.9:c.5593-44A>T ENSP00000315873.4:n.5593-44A>T
ENST00000295550.9:c.6211-44A>T MANE Select ENSP00000295550.4:n.6211-44A>T
ENST00000295550.8:c.6211-44A>T ENSP00000295550.4:n.6211-44A>T
ENST00000347401.7:c.4390-44A>T ENSP00000315609.4:n.4390-44A>T
ENST00000353578.8:c.5593-44A>T ENSP00000315873.4:n.5593-44A>T
ENST00000409809.5:c.5593-44A>T ENSP00000386844.1:n.5593-44A>T
ENST00000472056.5:c.4390-44A>T ENSP00000418285.1:n.4390-44A>T
NM_004369.3:c.6211-44A>T , LRG_473t1:c.6211-44A>T NP_004360.2:n.6211-44A>T
NM_057166.4:c.4390-44A>T NP_476507.3:n.4390-44A>T
NM_057167.3:c.5593-44A>T NP_476508.2:n.5593-44A>T
XM_005246065.1:c.5611-44A>T XP_005246122.1:n.5611-44A>T
XM_005246066.1:c.4990-44A>T XP_005246123.1:n.4990-44A>T
XM_006712253.1:c.5710-44A>T XP_006712316.1:n.5710-44A>T
XM_011510574.1:c.6208-44A>T XP_011508876.1:n.6208-44A>T
XM_011510575.1:c.3805-44A>T XP_011508877.1:n.3805-44A>T
XM_017003304.1:c.3805-44A>T XP_016858793.1:n.3805-44A>T
XM_024452684.1:c.4990-44A>T XP_024308452.1:n.4990-44A>T
NM_004369.4:c.6211-44A>T MANE Select NP_004360.2:n.6211-44A>T
NM_057166.5:c.4390-44A>T NP_476507.3:n.4390-44A>T
NM_057167.4:c.5593-44A>T NP_476508.2:n.5593-44A>T