Canonical Allele Identifier: CA431702054

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244992A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336349A>T , CM000664.2:g.237336349A>T	GRCh38
NC_000002.11:g.238244992A>T , CM000664.1:g.238244992A>T	GRCh37
NC_000002.10:g.237909731A>T	NCBI36
NG_008676.1:g.82859T>A , LRG_473:g.82859T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1396T>A
ENST00000353578.9:c.8133T>A	ENSP00000315873.4:p.Pro2711=
ENST00000682957.1:c.878T>A
ENST00000684508.1:n.1018T>A
ENST00000295550.9:c.8751T>A MANE Select	ENSP00000295550.4:p.Pro2917=
ENST00000295550.8:c.8751T>A	ENSP00000295550.4:p.Pro2917=
ENST00000347401.7:c.6927T>A	ENSP00000315609.4:p.Pro2309=
ENST00000353578.8:c.8133T>A	ENSP00000315873.4:p.Pro2711=
ENST00000409809.5:c.8133T>A	ENSP00000386844.1:p.Pro2711=
ENST00000472056.5:c.6930T>A	ENSP00000418285.1:p.Pro2310=
ENST00000491769.1:n.5193T>A
NM_004369.3:c.8751T>A , LRG_473t1:c.8751T>A	NP_004360.2:p.Pro2917=
NM_057166.4:c.6930T>A	NP_476507.3:p.Pro2310=
NM_057167.3:c.8133T>A	NP_476508.2:p.Pro2711=
XM_005246065.1:c.8151T>A	XP_005246122.1:p.Pro2717=
XM_005246066.1:c.7530T>A	XP_005246123.1:p.Pro2510=
XM_006712253.1:c.8250T>A	XP_006712316.1:p.Pro2750=
XM_011510574.1:c.8748T>A	XP_011508876.1:p.Pro2916=
XM_011510575.1:c.6345T>A	XP_011508877.1:p.Pro2115=
XM_017003304.1:c.6345T>A	XP_016858793.1:p.Pro2115=
XM_024452684.1:c.7530T>A	XP_024308452.1:p.Pro2510=
NM_004369.4:c.8751T>A MANE Select	NP_004360.2:p.Pro2917=
NM_057166.5:c.6930T>A	NP_476507.3:p.Pro2310=
NM_057167.4:c.8133T>A	NP_476508.2:p.Pro2711=