Canonical Allele Identifier: CA67832263

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237338678G>T , CM000664.2:g.237338678G>T	GRCh38
NC_000002.11:g.238247321G>T , CM000664.1:g.238247321G>T	GRCh37
NC_000002.10:g.237912060G>T	NCBI36
NG_008676.1:g.80530C>A , LRG_473:g.80530C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.8567+337C>A MANE Select	NP_004360.2:n.8567+337C>A
ENST00000295550.9:c.8567+337C>A MANE Select	ENSP00000295550.4:n.8567+337C>A
NM_004369.3:c.8567+337C>A , LRG_473t1:c.8567+337C>A	NP_004360.2:n.8567+337C>A
NM_057166.4:c.6746+337C>A	NP_476507.3:n.6746+337C>A
NM_057166.5:c.6746+337C>A	NP_476507.3:n.6746+337C>A
NM_057167.3:c.7949+337C>A	NP_476508.2:n.7949+337C>A
NM_057167.4:c.7949+337C>A	NP_476508.2:n.7949+337C>A
ENST00000295550.8:c.8567+337C>A	ENSP00000295550.4:n.8567+337C>A
ENST00000347401.7:c.6743+337C>A	ENSP00000315609.4:n.6743+337C>A
ENST00000347401.8:c.1212+337C>A
ENST00000353578.8:c.7949+337C>A	ENSP00000315873.4:n.7949+337C>A
ENST00000353578.9:c.7949+337C>A	ENSP00000315873.4:n.7949+337C>A
ENST00000409809.5:c.7949+337C>A	ENSP00000386844.1:n.7949+337C>A
ENST00000472056.5:c.6746+337C>A	ENSP00000418285.1:n.6746+337C>A
ENST00000491769.1:n.5009+337C>A
ENST00000682957.1:c.659C>A
ENST00000684508.1:n.834+337C>A
XM_005246065.1:c.7967+337C>A	XP_005246122.1:n.7967+337C>A
XM_005246066.1:c.7346+337C>A	XP_005246123.1:n.7346+337C>A
XM_006712253.1:c.8066+337C>A	XP_006712316.1:n.8066+337C>A
XM_011510574.1:c.8564+337C>A	XP_011508876.1:n.8564+337C>A
XM_011510575.1:c.6161+337C>A	XP_011508877.1:n.6161+337C>A
XM_017003304.1:c.6161+337C>A	XP_016858793.1:n.6161+337C>A
XM_024452684.1:c.7346+337C>A	XP_024308452.1:n.7346+337C>A