Canonical Allele Identifier: CA351190980

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244810G>T (hg19) ; chr2:g.237336167G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336167G>T , CM000664.2:g.237336167G>T	GRCh38
NC_000002.11:g.238244810G>T , CM000664.1:g.238244810G>T	GRCh37
NC_000002.10:g.237909549G>T	NCBI36
NG_008676.1:g.83041C>A , LRG_473:g.83041C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1578C>A
ENST00000353578.9:c.8315C>A	ENSP00000315873.4:p.Ala2772Asp
ENST00000682957.1:c.1060C>A
ENST00000684508.1:n.1200C>A
ENST00000295550.9:c.8933C>A MANE Select	ENSP00000295550.4:p.Ala2978Asp
ENST00000295550.8:c.8933C>A	ENSP00000295550.4:p.Ala2978Asp
ENST00000347401.7:c.7109C>A	ENSP00000315609.4:p.Ala2370Asp
ENST00000353578.8:c.8315C>A	ENSP00000315873.4:p.Ala2772Asp
ENST00000409809.5:c.8315C>A	ENSP00000386844.1:p.Ala2772Asp
ENST00000472056.5:c.7112C>A	ENSP00000418285.1:p.Ala2371Asp
ENST00000491769.1:n.5375C>A
NM_004369.3:c.8933C>A , LRG_473t1:c.8933C>A	NP_004360.2:p.Ala2978Asp
NM_057166.4:c.7112C>A	NP_476507.3:p.Ala2371Asp
NM_057167.3:c.8315C>A	NP_476508.2:p.Ala2772Asp
XM_005246065.1:c.8333C>A	XP_005246122.1:p.Ala2778Asp
XM_005246066.1:c.7712C>A	XP_005246123.1:p.Ala2571Asp
XM_006712253.1:c.8432C>A	XP_006712316.1:p.Ala2811Asp
XM_011510574.1:c.8930C>A	XP_011508876.1:p.Ala2977Asp
XM_011510575.1:c.6527C>A	XP_011508877.1:p.Ala2176Asp
XM_017003304.1:c.6527C>A	XP_016858793.1:p.Ala2176Asp
XM_024452684.1:c.7712C>A	XP_024308452.1:p.Ala2571Asp
NM_004369.4:c.8933C>A MANE Select	NP_004360.2:p.Ala2978Asp
NM_057166.5:c.7112C>A	NP_476507.3:p.Ala2371Asp
NM_057167.4:c.8315C>A	NP_476508.2:p.Ala2772Asp