Canonical Allele Identifier: CA431702308

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238245037C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336394C>T , CM000664.2:g.237336394C>T	GRCh38
NC_000002.11:g.238245037C>T , CM000664.1:g.238245037C>T	GRCh37
NC_000002.10:g.237909776C>T	NCBI36
NG_008676.1:g.82814G>A , LRG_473:g.82814G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1351G>A
ENST00000353578.9:c.8088G>A	ENSP00000315873.4:p.Gln2696=
ENST00000682957.1:c.833G>A
ENST00000684508.1:n.973G>A
ENST00000295550.9:c.8706G>A MANE Select	ENSP00000295550.4:p.Gln2902=
ENST00000295550.8:c.8706G>A	ENSP00000295550.4:p.Gln2902=
ENST00000347401.7:c.6882G>A	ENSP00000315609.4:p.Gln2294=
ENST00000353578.8:c.8088G>A	ENSP00000315873.4:p.Gln2696=
ENST00000409809.5:c.8088G>A	ENSP00000386844.1:p.Gln2696=
ENST00000472056.5:c.6885G>A	ENSP00000418285.1:p.Gln2295=
ENST00000491769.1:n.5148G>A
NM_004369.3:c.8706G>A , LRG_473t1:c.8706G>A	NP_004360.2:p.Gln2902=
NM_057166.4:c.6885G>A	NP_476507.3:p.Gln2295=
NM_057167.3:c.8088G>A	NP_476508.2:p.Gln2696=
XM_005246065.1:c.8106G>A	XP_005246122.1:p.Gln2702=
XM_005246066.1:c.7485G>A	XP_005246123.1:p.Gln2495=
XM_006712253.1:c.8205G>A	XP_006712316.1:p.Gln2735=
XM_011510574.1:c.8703G>A	XP_011508876.1:p.Gln2901=
XM_011510575.1:c.6300G>A	XP_011508877.1:p.Gln2100=
XM_017003304.1:c.6300G>A	XP_016858793.1:p.Gln2100=
XM_024452684.1:c.7485G>A	XP_024308452.1:p.Gln2495=
NM_004369.4:c.8706G>A MANE Select	NP_004360.2:p.Gln2902=
NM_057166.5:c.6885G>A	NP_476507.3:p.Gln2295=
NM_057167.4:c.8088G>A	NP_476508.2:p.Gln2696=