Canonical Allele Identifier: CA351201636

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238253021T>C (hg19) ; chr2:g.237344378T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344378T>C , CM000664.2:g.237344378T>C	GRCh38
NC_000002.11:g.238253021T>C , CM000664.1:g.238253021T>C	GRCh37
NC_000002.10:g.237917760T>C	NCBI36
NG_008676.1:g.74830A>G , LRG_473:g.74830A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.285A>G
ENST00000353578.9:c.7022A>G	ENSP00000315873.4:p.Glu2341Gly
ENST00000295550.9:c.7640A>G MANE Select	ENSP00000295550.4:p.Glu2547Gly
ENST00000295550.8:c.7640A>G	ENSP00000295550.4:p.Glu2547Gly
ENST00000347401.7:c.5816A>G	ENSP00000315609.4:p.Glu1939Gly
ENST00000353578.8:c.7022A>G	ENSP00000315873.4:p.Glu2341Gly
ENST00000409809.5:c.7022A>G	ENSP00000386844.1:p.Glu2341Gly
ENST00000472056.5:c.5819A>G	ENSP00000418285.1:p.Glu1940Gly
ENST00000491769.1:n.1894A>G
NM_004369.3:c.7640A>G , LRG_473t1:c.7640A>G	NP_004360.2:p.Glu2547Gly
NM_057166.4:c.5819A>G	NP_476507.3:p.Glu1940Gly
NM_057167.3:c.7022A>G	NP_476508.2:p.Glu2341Gly
XM_005246065.1:c.7040A>G	XP_005246122.1:p.Glu2347Gly
XM_005246066.1:c.6419A>G	XP_005246123.1:p.Glu2140Gly
XM_006712253.1:c.7139A>G	XP_006712316.1:p.Glu2380Gly
XM_011510574.1:c.7637A>G	XP_011508876.1:p.Glu2546Gly
XM_011510575.1:c.5234A>G	XP_011508877.1:p.Glu1745Gly
XM_017003304.1:c.5234A>G	XP_016858793.1:p.Glu1745Gly
XM_024452684.1:c.6419A>G	XP_024308452.1:p.Glu2140Gly
NM_004369.4:c.7640A>G MANE Select	NP_004360.2:p.Glu2547Gly
NM_057166.5:c.5819A>G	NP_476507.3:p.Glu1940Gly
NM_057167.4:c.7022A>G	NP_476508.2:p.Glu2341Gly