Canonical Allele Identifier: CA2189600

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237381261G>C , CM000664.2:g.237381261G>C	GRCh38
NC_000002.11:g.238289904G>C , CM000664.1:g.238289904G>C	GRCh37
NC_000002.10:g.237954643G>C	NCBI36
NG_008676.1:g.37947C>G , LRG_473:g.37947C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.1551C>G MANE Select	NP_004360.2:p.Pro517=
ENST00000295550.9:c.1551C>G MANE Select	ENSP00000295550.4:p.Pro517=
NM_004369.3:c.1551C>G , LRG_473t1:c.1551C>G	NP_004360.2:p.Pro517=
NM_057164.4:c.330C>G	NP_476505.3:p.Pro110=
NM_057164.5:c.330C>G	NP_476505.3:p.Pro110=
NM_057165.4:c.933C>G	NP_476506.3:p.Pro311=
NM_057165.5:c.933C>G	NP_476506.3:p.Pro311=
NM_057166.4:c.330C>G	NP_476507.3:p.Pro110=
NM_057166.5:c.330C>G	NP_476507.3:p.Pro110=
NM_057167.3:c.933C>G	NP_476508.2:p.Pro311=
NM_057167.4:c.933C>G	NP_476508.2:p.Pro311=
ENST00000295550.8:c.1551C>G	ENSP00000295550.4:p.Pro517=
ENST00000347401.7:c.330C>G	ENSP00000315609.4:p.Pro110=
ENST00000353578.8:c.933C>G	ENSP00000315873.4:p.Pro311=
ENST00000353578.9:c.933C>G	ENSP00000315873.4:p.Pro311=
ENST00000392003.6:c.330C>G	ENSP00000375860.2:p.Pro110=
ENST00000392004.7:c.933C>G	ENSP00000375861.3:p.Pro311=
ENST00000409809.5:c.933C>G	ENSP00000386844.1:p.Pro311=
ENST00000433762.1:c.1551C>G	ENSP00000389539.1:p.Pro517=
ENST00000472056.5:c.330C>G	ENSP00000418285.1:p.Pro110=
XM_005246065.1:c.1551C>G	XP_005246122.1:p.Pro517=
XM_005246066.1:c.330C>G	XP_005246123.1:p.Pro110=
XM_006712253.1:c.1551C>G	XP_006712316.1:p.Pro517=
XM_011510574.1:c.1551C>G	XP_011508876.1:p.Pro517=
XM_011510575.1:c.92-3917C>G	XP_011508877.1:n.92-3917C>G
XM_017003304.1:c.92-3917C>G	XP_016858793.1:n.92-3917C>G
XM_024452684.1:c.330C>G	XP_024308452.1:p.Pro110=