Canonical Allele Identifier: CA351190841

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244776A>T (hg19) ; chr2:g.237336133A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336133A>T , CM000664.2:g.237336133A>T	GRCh38
NC_000002.11:g.238244776A>T , CM000664.1:g.238244776A>T	GRCh37
NC_000002.10:g.237909515A>T	NCBI36
NG_008676.1:g.83075T>A , LRG_473:g.83075T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1610+2T>A
ENST00000353578.9:c.8347+2T>A	ENSP00000315873.4:n.8347+2T>A
ENST00000682957.1:c.1092+2T>A
ENST00000684508.1:n.1234T>A
ENST00000295550.9:c.8965+2T>A MANE Select	ENSP00000295550.4:n.8965+2T>A
ENST00000295550.8:c.8965+2T>A	ENSP00000295550.4:n.8965+2T>A
ENST00000347401.7:c.7141+2T>A	ENSP00000315609.4:n.7141+2T>A
ENST00000353578.8:c.8347+2T>A	ENSP00000315873.4:n.8347+2T>A
ENST00000409809.5:c.8347+2T>A	ENSP00000386844.1:n.8347+2T>A
ENST00000472056.5:c.7144+2T>A	ENSP00000418285.1:n.7144+2T>A
ENST00000491769.1:n.5407+2T>A
NM_004369.3:c.8965+2T>A , LRG_473t1:c.8965+2T>A	NP_004360.2:n.8965+2T>A
NM_057166.4:c.7144+2T>A	NP_476507.3:n.7144+2T>A
NM_057167.3:c.8347+2T>A	NP_476508.2:n.8347+2T>A
XM_005246065.1:c.8365+2T>A	XP_005246122.1:n.8365+2T>A
XM_005246066.1:c.7744+2T>A	XP_005246123.1:n.7744+2T>A
XM_006712253.1:c.8464+2T>A	XP_006712316.1:n.8464+2T>A
XM_011510574.1:c.8962+2T>A	XP_011508876.1:n.8962+2T>A
XM_011510575.1:c.6559+2T>A	XP_011508877.1:n.6559+2T>A
XM_017003304.1:c.6559+2T>A	XP_016858793.1:n.6559+2T>A
XM_024452684.1:c.7744+2T>A	XP_024308452.1:n.7744+2T>A
NM_004369.4:c.8965+2T>A MANE Select	NP_004360.2:n.8965+2T>A
NM_057166.5:c.7144+2T>A	NP_476507.3:n.7144+2T>A
NM_057167.4:c.8347+2T>A	NP_476508.2:n.8347+2T>A