Canonical Allele Identifier: CA1043803317

Gene: COL6A3

Linked Data

• gnomAD v3: 2-237359327-T-A
• gnomAD v4: 2-237359327-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237359327T>A , CM000664.2:g.237359327T>A	GRCh38
NC_000002.11:g.238267970T>A , CM000664.1:g.238267970T>A	GRCh37
NC_000002.10:g.237932709T>A	NCBI36
NG_008676.1:g.59881A>T , LRG_473:g.59881A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.5691+35A>T	ENSP00000315873.4:n.5691+35A>T
ENST00000295550.9:c.6309+35A>T MANE Select	ENSP00000295550.4:n.6309+35A>T
ENST00000295550.8:c.6309+35A>T	ENSP00000295550.4:n.6309+35A>T
ENST00000347401.7:c.4488+35A>T	ENSP00000315609.4:n.4488+35A>T
ENST00000353578.8:c.5691+35A>T	ENSP00000315873.4:n.5691+35A>T
ENST00000409809.5:c.5691+35A>T	ENSP00000386844.1:n.5691+35A>T
ENST00000472056.5:c.4488+35A>T	ENSP00000418285.1:n.4488+35A>T
NM_004369.3:c.6309+35A>T , LRG_473t1:c.6309+35A>T	NP_004360.2:n.6309+35A>T
NM_057166.4:c.4488+35A>T	NP_476507.3:n.4488+35A>T
NM_057167.3:c.5691+35A>T	NP_476508.2:n.5691+35A>T
XM_005246065.1:c.5709+35A>T	XP_005246122.1:n.5709+35A>T
XM_005246066.1:c.5088+35A>T	XP_005246123.1:n.5088+35A>T
XM_006712253.1:c.5808+35A>T	XP_006712316.1:n.5808+35A>T
XM_011510574.1:c.6306+35A>T	XP_011508876.1:n.6306+35A>T
XM_011510575.1:c.3903+35A>T	XP_011508877.1:n.3903+35A>T
XM_017003304.1:c.3903+35A>T	XP_016858793.1:n.3903+35A>T
XM_024452684.1:c.5088+35A>T	XP_024308452.1:n.5088+35A>T
NM_004369.4:c.6309+35A>T MANE Select	NP_004360.2:n.6309+35A>T
NM_057166.5:c.4488+35A>T	NP_476507.3:n.4488+35A>T
NM_057167.4:c.5691+35A>T	NP_476508.2:n.5691+35A>T