Canonical Allele Identifier: CA351202639

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238253169T>G (hg19) ; chr2:g.237344526T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344526T>G , CM000664.2:g.237344526T>G	GRCh38
NC_000002.11:g.238253169T>G , CM000664.1:g.238253169T>G	GRCh37
NC_000002.10:g.237917908T>G	NCBI36
NG_008676.1:g.74682A>C , LRG_473:g.74682A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.137A>C
ENST00000353578.9:c.6874A>C	ENSP00000315873.4:p.Thr2292Pro
ENST00000295550.9:c.7492A>C MANE Select	ENSP00000295550.4:p.Thr2498Pro
ENST00000295550.8:c.7492A>C	ENSP00000295550.4:p.Thr2498Pro
ENST00000347401.7:c.5668A>C	ENSP00000315609.4:p.Thr1890Pro
ENST00000353578.8:c.6874A>C	ENSP00000315873.4:p.Thr2292Pro
ENST00000409809.5:c.6874A>C	ENSP00000386844.1:p.Thr2292Pro
ENST00000472056.5:c.5671A>C	ENSP00000418285.1:p.Thr1891Pro
ENST00000491769.1:n.1746A>C
NM_004369.3:c.7492A>C , LRG_473t1:c.7492A>C	NP_004360.2:p.Thr2498Pro
NM_057166.4:c.5671A>C	NP_476507.3:p.Thr1891Pro
NM_057167.3:c.6874A>C	NP_476508.2:p.Thr2292Pro
XM_005246065.1:c.6892A>C	XP_005246122.1:p.Thr2298Pro
XM_005246066.1:c.6271A>C	XP_005246123.1:p.Thr2091Pro
XM_006712253.1:c.6991A>C	XP_006712316.1:p.Thr2331Pro
XM_011510574.1:c.7489A>C	XP_011508876.1:p.Thr2497Pro
XM_011510575.1:c.5086A>C	XP_011508877.1:p.Thr1696Pro
XM_017003304.1:c.5086A>C	XP_016858793.1:p.Thr1696Pro
XM_024452684.1:c.6271A>C	XP_024308452.1:p.Thr2091Pro
NM_004369.4:c.7492A>C MANE Select	NP_004360.2:p.Thr2498Pro
NM_057166.5:c.5671A>C	NP_476507.3:p.Thr1891Pro
NM_057167.4:c.6874A>C	NP_476508.2:p.Thr2292Pro