Canonical Allele Identifier: CA351191181

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244867G>T (hg19) ; chr2:g.237336224G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336224G>T , CM000664.2:g.237336224G>T	GRCh38
NC_000002.11:g.238244867G>T , CM000664.1:g.238244867G>T	GRCh37
NC_000002.10:g.237909606G>T	NCBI36
NG_008676.1:g.82984C>A , LRG_473:g.82984C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1521C>A
ENST00000353578.9:c.8258C>A	ENSP00000315873.4:p.Ala2753Asp
ENST00000682957.1:c.1003C>A
ENST00000684508.1:n.1143C>A
ENST00000295550.9:c.8876C>A MANE Select	ENSP00000295550.4:p.Ala2959Asp
ENST00000295550.8:c.8876C>A	ENSP00000295550.4:p.Ala2959Asp
ENST00000347401.7:c.7052C>A	ENSP00000315609.4:p.Ala2351Asp
ENST00000353578.8:c.8258C>A	ENSP00000315873.4:p.Ala2753Asp
ENST00000409809.5:c.8258C>A	ENSP00000386844.1:p.Ala2753Asp
ENST00000472056.5:c.7055C>A	ENSP00000418285.1:p.Ala2352Asp
ENST00000491769.1:n.5318C>A
NM_004369.3:c.8876C>A , LRG_473t1:c.8876C>A	NP_004360.2:p.Ala2959Asp
NM_057166.4:c.7055C>A	NP_476507.3:p.Ala2352Asp
NM_057167.3:c.8258C>A	NP_476508.2:p.Ala2753Asp
XM_005246065.1:c.8276C>A	XP_005246122.1:p.Ala2759Asp
XM_005246066.1:c.7655C>A	XP_005246123.1:p.Ala2552Asp
XM_006712253.1:c.8375C>A	XP_006712316.1:p.Ala2792Asp
XM_011510574.1:c.8873C>A	XP_011508876.1:p.Ala2958Asp
XM_011510575.1:c.6470C>A	XP_011508877.1:p.Ala2157Asp
XM_017003304.1:c.6470C>A	XP_016858793.1:p.Ala2157Asp
XM_024452684.1:c.7655C>A	XP_024308452.1:p.Ala2552Asp
NM_004369.4:c.8876C>A MANE Select	NP_004360.2:p.Ala2959Asp
NM_057166.5:c.7055C>A	NP_476507.3:p.Ala2352Asp
NM_057167.4:c.8258C>A	NP_476508.2:p.Ala2753Asp