Canonical Allele Identifier: CA1337618452
Gene: COL6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237361039T= , CM000664.2:g.237361039T= GRCh38
NC_000002.11:g.238269682T= , CM000664.1:g.238269682T= GRCh37
NC_000002.10:g.237934421T= NCBI36
NG_008676.1:g.58169A= , LRG_473:g.58169A=

Transcript Alleles

HGVS Amino-acid change
ENST00000353578.9:c.5592+82A= ENSP00000315873.4:n.5592+82A=
ENST00000295550.9:c.6210+82A= MANE Select ENSP00000295550.4:n.6210+82A=
ENST00000295550.8:c.6210+82A= ENSP00000295550.4:n.6210+82A=
ENST00000347401.7:c.4389+82A= ENSP00000315609.4:n.4389+82A=
ENST00000353578.8:c.5592+82A= ENSP00000315873.4:n.5592+82A=
ENST00000409809.5:c.5592+82A= ENSP00000386844.1:n.5592+82A=
ENST00000472056.5:c.4389+82A= ENSP00000418285.1:n.4389+82A=
NM_004369.3:c.6210+82A= , LRG_473t1:c.6210+82A= NP_004360.2:n.6210+82A=
NM_057166.4:c.4389+82A= NP_476507.3:n.4389+82A=
NM_057167.3:c.5592+82A= NP_476508.2:n.5592+82A=
XM_005246065.1:c.5610+82A= XP_005246122.1:n.5610+82A=
XM_005246066.1:c.4989+82A= XP_005246123.1:n.4989+82A=
XM_006712253.1:c.5709+82A= XP_006712316.1:n.5709+82A=
XM_011510574.1:c.6207+82A= XP_011508876.1:n.6207+82A=
XM_011510575.1:c.3804+82A= XP_011508877.1:n.3804+82A=
XM_017003304.1:c.3804+82A= XP_016858793.1:n.3804+82A=
XM_024452684.1:c.4989+82A= XP_024308452.1:n.4989+82A=
NM_004369.4:c.6210+82A= MANE Select NP_004360.2:n.6210+82A=
NM_057166.5:c.4389+82A= NP_476507.3:n.4389+82A=
NM_057167.4:c.5592+82A= NP_476508.2:n.5592+82A=