Canonical Allele Identifier: CA1337620958
Gene: COL6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237366913A= , CM000664.2:g.237366913A= GRCh38
NC_000002.11:g.238275556A= , CM000664.1:g.238275556A= GRCh37
NC_000002.10:g.237940295A= NCBI36
NG_008676.1:g.52295T= , LRG_473:g.52295T=

Transcript Alleles

HGVS Amino-acid change
ENST00000353578.9:c.4656T= ENSP00000315873.4:p.Asp1552=
ENST00000295550.9:c.5274T= MANE Select ENSP00000295550.4:p.Asp1758=
ENST00000295550.8:c.5274T= ENSP00000295550.4:p.Asp1758=
ENST00000347401.7:c.3453T= ENSP00000315609.4:p.Asp1151=
ENST00000353578.8:c.4656T= ENSP00000315873.4:p.Asp1552=
ENST00000409809.5:c.4656T= ENSP00000386844.1:p.Asp1552=
ENST00000472056.5:c.3453T= ENSP00000418285.1:p.Asp1151=
NM_004369.3:c.5274T= , LRG_473t1:c.5274T= NP_004360.2:p.Asp1758=
NM_057166.4:c.3453T= NP_476507.3:p.Asp1151=
NM_057167.3:c.4656T= NP_476508.2:p.Asp1552=
XM_005246065.1:c.4674T= XP_005246122.1:p.Asp1558=
XM_005246066.1:c.4053T= XP_005246123.1:p.Asp1351=
XM_006712253.1:c.4773T= XP_006712316.1:p.Asp1591=
XM_011510574.1:c.5271T= XP_011508876.1:p.Asp1757=
XM_011510575.1:c.2868T= XP_011508877.1:p.Asp956=
XM_017003304.1:c.2868T= XP_016858793.1:p.Asp956=
XM_024452684.1:c.4053T= XP_024308452.1:p.Asp1351=
NM_004369.4:c.5274T= MANE Select NP_004360.2:p.Asp1758=
NM_057166.5:c.3453T= NP_476507.3:p.Asp1151=
NM_057167.4:c.4656T= NP_476508.2:p.Asp1552=