Canonical Allele Identifier: CA2188425

Gene: COL6A3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237361156C>T , CM000664.2:g.237361156C>T	GRCh38
NC_000002.11:g.238269799C>T , CM000664.1:g.238269799C>T	GRCh37
NC_000002.10:g.237934538C>T	NCBI36
NG_008676.1:g.58052G>A , LRG_473:g.58052G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.5557G>A	ENSP00000315873.4:p.Gly1853Ser
ENST00000295550.9:c.6175G>A MANE Select	ENSP00000295550.4:p.Gly2059Ser
ENST00000295550.8:c.6175G>A	ENSP00000295550.4:p.Gly2059Ser
ENST00000347401.7:c.4354G>A	ENSP00000315609.4:p.Gly1452Ser
ENST00000353578.8:c.5557G>A	ENSP00000315873.4:p.Gly1853Ser
ENST00000409809.5:c.5557G>A	ENSP00000386844.1:p.Gly1853Ser
ENST00000472056.5:c.4354G>A	ENSP00000418285.1:p.Gly1452Ser
NM_004369.3:c.6175G>A , LRG_473t1:c.6175G>A	NP_004360.2:p.Gly2059Ser
NM_057166.4:c.4354G>A	NP_476507.3:p.Gly1452Ser
NM_057167.3:c.5557G>A	NP_476508.2:p.Gly1853Ser
XM_005246065.1:c.5575G>A	XP_005246122.1:p.Gly1859Ser
XM_005246066.1:c.4954G>A	XP_005246123.1:p.Gly1652Ser
XM_006712253.1:c.5674G>A	XP_006712316.1:p.Gly1892Ser
XM_011510574.1:c.6172G>A	XP_011508876.1:p.Gly2058Ser
XM_011510575.1:c.3769G>A	XP_011508877.1:p.Gly1257Ser
XM_017003304.1:c.3769G>A	XP_016858793.1:p.Gly1257Ser
XM_024452684.1:c.4954G>A	XP_024308452.1:p.Gly1652Ser
NM_004369.4:c.6175G>A MANE Select	NP_004360.2:p.Gly2059Ser
NM_057166.5:c.4354G>A	NP_476507.3:p.Gly1452Ser
NM_057167.4:c.5557G>A	NP_476508.2:p.Gly1853Ser