Canonical Allele Identifier: CA431675101

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238249120C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237340477C>A , CM000664.2:g.237340477C>A	GRCh38
NC_000002.11:g.238249120C>A , CM000664.1:g.238249120C>A	GRCh37
NC_000002.10:g.237913859C>A	NCBI36
NG_008676.1:g.78731G>T , LRG_473:g.78731G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1084G>T
ENST00000353578.9:c.7821G>T	ENSP00000315873.4:p.Gly2607=
ENST00000682957.1:c.442G>T
ENST00000684508.1:n.706G>T
ENST00000295550.9:c.8439G>T MANE Select	ENSP00000295550.4:p.Gly2813=
ENST00000295550.8:c.8439G>T	ENSP00000295550.4:p.Gly2813=
ENST00000347401.7:c.6615G>T	ENSP00000315609.4:p.Gly2205=
ENST00000353578.8:c.7821G>T	ENSP00000315873.4:p.Gly2607=
ENST00000409809.5:c.7821G>T	ENSP00000386844.1:p.Gly2607=
ENST00000468792.1:n.126G>T
ENST00000472056.5:c.6618G>T	ENSP00000418285.1:p.Gly2206=
ENST00000491769.1:n.4881G>T
NM_004369.3:c.8439G>T , LRG_473t1:c.8439G>T	NP_004360.2:p.Gly2813=
NM_057166.4:c.6618G>T	NP_476507.3:p.Gly2206=
NM_057167.3:c.7821G>T	NP_476508.2:p.Gly2607=
XM_005246065.1:c.7839G>T	XP_005246122.1:p.Gly2613=
XM_005246066.1:c.7218G>T	XP_005246123.1:p.Gly2406=
XM_006712253.1:c.7938G>T	XP_006712316.1:p.Gly2646=
XM_011510574.1:c.8436G>T	XP_011508876.1:p.Gly2812=
XM_011510575.1:c.6033G>T	XP_011508877.1:p.Gly2011=
XM_017003304.1:c.6033G>T	XP_016858793.1:p.Gly2011=
XM_024452684.1:c.7218G>T	XP_024308452.1:p.Gly2406=
NM_004369.4:c.8439G>T MANE Select	NP_004360.2:p.Gly2813=
NM_057166.5:c.6618G>T	NP_476507.3:p.Gly2206=
NM_057167.4:c.7821G>T	NP_476508.2:p.Gly2607=