Canonical Allele Identifier: CA2187766

Gene: COL6A3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344410C>T , CM000664.2:g.237344410C>T	GRCh38
NC_000002.11:g.238253053C>T , CM000664.1:g.238253053C>T	GRCh37
NC_000002.10:g.237917792C>T	NCBI36
NG_008676.1:g.74798G>A , LRG_473:g.74798G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004369.4:c.7608G>A MANE Select	NP_004360.2:p.Ala2536=
ENST00000295550.9:c.7608G>A MANE Select	ENSP00000295550.4:p.Ala2536=
NM_004369.3:c.7608G>A , LRG_473t1:c.7608G>A	NP_004360.2:p.Ala2536=
NM_057166.4:c.5787G>A	NP_476507.3:p.Ala1929=
NM_057166.5:c.5787G>A	NP_476507.3:p.Ala1929=
NM_057167.3:c.6990G>A	NP_476508.2:p.Ala2330=
NM_057167.4:c.6990G>A	NP_476508.2:p.Ala2330=
ENST00000295550.8:c.7608G>A	ENSP00000295550.4:p.Ala2536=
ENST00000347401.7:c.5784G>A	ENSP00000315609.4:p.Ala1928=
ENST00000347401.8:c.253G>A
ENST00000353578.8:c.6990G>A	ENSP00000315873.4:p.Ala2330=
ENST00000353578.9:c.6990G>A	ENSP00000315873.4:p.Ala2330=
ENST00000409809.5:c.6990G>A	ENSP00000386844.1:p.Ala2330=
ENST00000472056.5:c.5787G>A	ENSP00000418285.1:p.Ala1929=
ENST00000491769.1:n.1862G>A
XM_005246065.1:c.7008G>A	XP_005246122.1:p.Ala2336=
XM_005246066.1:c.6387G>A	XP_005246123.1:p.Ala2129=
XM_006712253.1:c.7107G>A	XP_006712316.1:p.Ala2369=
XM_011510574.1:c.7605G>A	XP_011508876.1:p.Ala2535=
XM_011510575.1:c.5202G>A	XP_011508877.1:p.Ala1734=
XM_017003304.1:c.5202G>A	XP_016858793.1:p.Ala1734=
XM_024452684.1:c.6387G>A	XP_024308452.1:p.Ala2129=