Canonical Allele Identifier: CA351190999
Gene: COL6A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237336172T>A , CM000664.2:g.237336172T>A GRCh38
NC_000002.11:g.238244815T>A , CM000664.1:g.238244815T>A GRCh37
NC_000002.10:g.237909554T>A NCBI36
NG_008676.1:g.83036A>T , LRG_473:g.83036A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000347401.8:c.1573A>T
ENST00000353578.9:c.8310A>T ENSP00000315873.4:p.Lys2770Asn
ENST00000682957.1:c.1055A>T
ENST00000684508.1:n.1195A>T
ENST00000295550.9:c.8928A>T MANE Select ENSP00000295550.4:p.Lys2976Asn
ENST00000295550.8:c.8928A>T ENSP00000295550.4:p.Lys2976Asn
ENST00000347401.7:c.7104A>T ENSP00000315609.4:p.Lys2368Asn
ENST00000353578.8:c.8310A>T ENSP00000315873.4:p.Lys2770Asn
ENST00000409809.5:c.8310A>T ENSP00000386844.1:p.Lys2770Asn
ENST00000472056.5:c.7107A>T ENSP00000418285.1:p.Lys2369Asn
ENST00000491769.1:n.5370A>T
NM_004369.3:c.8928A>T , LRG_473t1:c.8928A>T NP_004360.2:p.Lys2976Asn
NM_057166.4:c.7107A>T NP_476507.3:p.Lys2369Asn
NM_057167.3:c.8310A>T NP_476508.2:p.Lys2770Asn
XM_005246065.1:c.8328A>T XP_005246122.1:p.Lys2776Asn
XM_005246066.1:c.7707A>T XP_005246123.1:p.Lys2569Asn
XM_006712253.1:c.8427A>T XP_006712316.1:p.Lys2809Asn
XM_011510574.1:c.8925A>T XP_011508876.1:p.Lys2975Asn
XM_011510575.1:c.6522A>T XP_011508877.1:p.Lys2174Asn
XM_017003304.1:c.6522A>T XP_016858793.1:p.Lys2174Asn
XM_024452684.1:c.7707A>T XP_024308452.1:p.Lys2569Asn
NM_004369.4:c.8928A>T MANE Select NP_004360.2:p.Lys2976Asn
NM_057166.5:c.7107A>T NP_476507.3:p.Lys2369Asn
NM_057167.4:c.8310A>T NP_476508.2:p.Lys2770Asn