Canonical Allele Identifier: CA2187292
Community Standard Title: NM_004369.4(COL6A3):c.9329-7A>T
Gene: COL6A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237325731T>A , CM000664.2:g.237325731T>A GRCh38
NC_000002.11:g.238234374T>A , CM000664.1:g.238234374T>A GRCh37
NC_000002.10:g.237899113T>A NCBI36
NG_008676.1:g.93477A>T , LRG_473:g.93477A>T

Transcript Alleles

HGVS Amino-acid Change
NM_004369.4:c.9329-7A>T MANE Select NP_004360.2:n.9329-7A>T
ENST00000295550.9:c.9329-7A>T MANE Select ENSP00000295550.4:n.9329-7A>T
NM_004369.3:c.9329-7A>T , LRG_473t1:c.9329-7A>T NP_004360.2:n.9329-7A>T
NM_057166.4:c.7508-7A>T NP_476507.3:n.7508-7A>T
NM_057166.5:c.7508-7A>T NP_476507.3:n.7508-7A>T
NM_057167.3:c.8711-7A>T NP_476508.2:n.8711-7A>T
NM_057167.4:c.8711-7A>T NP_476508.2:n.8711-7A>T
ENST00000295550.8:c.9329-7A>T ENSP00000295550.4:n.9329-7A>T
ENST00000347401.7:c.7505-7A>T ENSP00000315609.4:n.7505-7A>T
ENST00000347401.8:c.1710-7A>T
ENST00000353578.8:c.8711-7A>T ENSP00000315873.4:n.8711-7A>T
ENST00000353578.9:c.8711-7A>T ENSP00000315873.4:n.8711-7A>T
ENST00000409809.5:c.8711-7A>T ENSP00000386844.1:n.8711-7A>T
ENST00000472056.5:c.7508-7A>T ENSP00000418285.1:n.7508-7A>T
ENST00000473258.1:n.4450A>T
ENST00000491769.1:n.5771-7A>T
ENST00000682957.1:c.1456-7A>T
ENST00000683348.1:c.195-7A>T ENSP00000508058.1:n.195-7A>T
XM_005246065.1:c.8729-7A>T XP_005246122.1:n.8729-7A>T
XM_005246066.1:c.8108-7A>T XP_005246123.1:n.8108-7A>T
XM_006712253.1:c.8828-7A>T XP_006712316.1:n.8828-7A>T
XM_011510574.1:c.9326-7A>T XP_011508876.1:n.9326-7A>T
XM_011510575.1:c.6923-7A>T XP_011508877.1:n.6923-7A>T
XM_017003304.1:c.6923-7A>T XP_016858793.1:n.6923-7A>T
XM_024452684.1:c.8108-7A>T XP_024308452.1:n.8108-7A>T