Canonical Allele Identifier: CA431702490

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238245070G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336427G>A , CM000664.2:g.237336427G>A	GRCh38
NC_000002.11:g.238245070G>A , CM000664.1:g.238245070G>A	GRCh37
NC_000002.10:g.237909809G>A	NCBI36
NG_008676.1:g.82781C>T , LRG_473:g.82781C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1318C>T
ENST00000353578.9:c.8055C>T	ENSP00000315873.4:p.Thr2685=
ENST00000682957.1:c.800C>T
ENST00000684508.1:n.940C>T
ENST00000295550.9:c.8673C>T MANE Select	ENSP00000295550.4:p.Thr2891=
ENST00000295550.8:c.8673C>T	ENSP00000295550.4:p.Thr2891=
ENST00000347401.7:c.6849C>T	ENSP00000315609.4:p.Thr2283=
ENST00000353578.8:c.8055C>T	ENSP00000315873.4:p.Thr2685=
ENST00000409809.5:c.8055C>T	ENSP00000386844.1:p.Thr2685=
ENST00000472056.5:c.6852C>T	ENSP00000418285.1:p.Thr2284=
ENST00000491769.1:n.5115C>T
NM_004369.3:c.8673C>T , LRG_473t1:c.8673C>T	NP_004360.2:p.Thr2891=
NM_057166.4:c.6852C>T	NP_476507.3:p.Thr2284=
NM_057167.3:c.8055C>T	NP_476508.2:p.Thr2685=
XM_005246065.1:c.8073C>T	XP_005246122.1:p.Thr2691=
XM_005246066.1:c.7452C>T	XP_005246123.1:p.Thr2484=
XM_006712253.1:c.8172C>T	XP_006712316.1:p.Thr2724=
XM_011510574.1:c.8670C>T	XP_011508876.1:p.Thr2890=
XM_011510575.1:c.6267C>T	XP_011508877.1:p.Thr2089=
XM_017003304.1:c.6267C>T	XP_016858793.1:p.Thr2089=
XM_024452684.1:c.7452C>T	XP_024308452.1:p.Thr2484=
NM_004369.4:c.8673C>T MANE Select	NP_004360.2:p.Thr2891=
NM_057166.5:c.6852C>T	NP_476507.3:p.Thr2284=
NM_057167.4:c.8055C>T	NP_476508.2:p.Thr2685=