Canonical Allele Identifier: CA2187757
Community Standard Title: NM_004369.4(COL6A3):c.7646G>A (p.Arg2549Gln)
Gene: COL6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237344372C>T , CM000664.2:g.237344372C>T GRCh38
NC_000002.11:g.238253015C>T , CM000664.1:g.238253015C>T GRCh37
NC_000002.10:g.237917754C>T NCBI36
NG_008676.1:g.74836G>A , LRG_473:g.74836G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004369.4:c.7646G>A MANE Select NP_004360.2:p.Arg2549Gln
ENST00000295550.9:c.7646G>A MANE Select ENSP00000295550.4:p.Arg2549Gln
NM_004369.3:c.7646G>A , LRG_473t1:c.7646G>A NP_004360.2:p.Arg2549Gln
NM_057166.4:c.5825G>A NP_476507.3:p.Arg1942Gln
NM_057166.5:c.5825G>A NP_476507.3:p.Arg1942Gln
NM_057167.3:c.7028G>A NP_476508.2:p.Arg2343Gln
NM_057167.4:c.7028G>A NP_476508.2:p.Arg2343Gln
ENST00000295550.8:c.7646G>A ENSP00000295550.4:p.Arg2549Gln
ENST00000347401.7:c.5822G>A ENSP00000315609.4:p.Arg1941Gln
ENST00000347401.8:c.291G>A
ENST00000353578.8:c.7028G>A ENSP00000315873.4:p.Arg2343Gln
ENST00000353578.9:c.7028G>A ENSP00000315873.4:p.Arg2343Gln
ENST00000409809.5:c.7028G>A ENSP00000386844.1:p.Arg2343Gln
ENST00000472056.5:c.5825G>A ENSP00000418285.1:p.Arg1942Gln
ENST00000491769.1:n.1900G>A
XM_005246065.1:c.7046G>A XP_005246122.1:p.Arg2349Gln
XM_005246066.1:c.6425G>A XP_005246123.1:p.Arg2142Gln
XM_006712253.1:c.7145G>A XP_006712316.1:p.Arg2382Gln
XM_011510574.1:c.7643G>A XP_011508876.1:p.Arg2548Gln
XM_011510575.1:c.5240G>A XP_011508877.1:p.Arg1747Gln
XM_017003304.1:c.5240G>A XP_016858793.1:p.Arg1747Gln
XM_024452684.1:c.6425G>A XP_024308452.1:p.Arg2142Gln