Canonical Allele Identifier: CA351187895

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238275591C>T (hg19) ; chr2:g.237366948C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237366948C>T , CM000664.2:g.237366948C>T	GRCh38
NC_000002.11:g.238275591C>T , CM000664.1:g.238275591C>T	GRCh37
NC_000002.10:g.237940330C>T	NCBI36
NG_008676.1:g.52260G>A , LRG_473:g.52260G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.4621G>A	ENSP00000315873.4:p.Ala1541Thr
ENST00000295550.9:c.5239G>A MANE Select	ENSP00000295550.4:p.Ala1747Thr
ENST00000295550.8:c.5239G>A	ENSP00000295550.4:p.Ala1747Thr
ENST00000347401.7:c.3418G>A	ENSP00000315609.4:p.Ala1140Thr
ENST00000353578.8:c.4621G>A	ENSP00000315873.4:p.Ala1541Thr
ENST00000409809.5:c.4621G>A	ENSP00000386844.1:p.Ala1541Thr
ENST00000472056.5:c.3418G>A	ENSP00000418285.1:p.Ala1140Thr
NM_004369.3:c.5239G>A , LRG_473t1:c.5239G>A	NP_004360.2:p.Ala1747Thr
NM_057166.4:c.3418G>A	NP_476507.3:p.Ala1140Thr
NM_057167.3:c.4621G>A	NP_476508.2:p.Ala1541Thr
XM_005246065.1:c.4639G>A	XP_005246122.1:p.Ala1547Thr
XM_005246066.1:c.4018G>A	XP_005246123.1:p.Ala1340Thr
XM_006712253.1:c.4738G>A	XP_006712316.1:p.Ala1580Thr
XM_011510574.1:c.5236G>A	XP_011508876.1:p.Ala1746Thr
XM_011510575.1:c.2833G>A	XP_011508877.1:p.Ala945Thr
XM_017003304.1:c.2833G>A	XP_016858793.1:p.Ala945Thr
XM_024452684.1:c.4018G>A	XP_024308452.1:p.Ala1340Thr
NM_004369.4:c.5239G>A MANE Select	NP_004360.2:p.Ala1747Thr
NM_057166.5:c.3418G>A	NP_476507.3:p.Ala1140Thr
NM_057167.4:c.4621G>A	NP_476508.2:p.Ala1541Thr