Canonical Allele Identifier: CA351191004

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244816T>G (hg19) ; chr2:g.237336173T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336173T>G , CM000664.2:g.237336173T>G	GRCh38
NC_000002.11:g.238244816T>G , CM000664.1:g.238244816T>G	GRCh37
NC_000002.10:g.237909555T>G	NCBI36
NG_008676.1:g.83035A>C , LRG_473:g.83035A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1572A>C
ENST00000353578.9:c.8309A>C	ENSP00000315873.4:p.Lys2770Thr
ENST00000682957.1:c.1054A>C
ENST00000684508.1:n.1194A>C
ENST00000295550.9:c.8927A>C MANE Select	ENSP00000295550.4:p.Lys2976Thr
ENST00000295550.8:c.8927A>C	ENSP00000295550.4:p.Lys2976Thr
ENST00000347401.7:c.7103A>C	ENSP00000315609.4:p.Lys2368Thr
ENST00000353578.8:c.8309A>C	ENSP00000315873.4:p.Lys2770Thr
ENST00000409809.5:c.8309A>C	ENSP00000386844.1:p.Lys2770Thr
ENST00000472056.5:c.7106A>C	ENSP00000418285.1:p.Lys2369Thr
ENST00000491769.1:n.5369A>C
NM_004369.3:c.8927A>C , LRG_473t1:c.8927A>C	NP_004360.2:p.Lys2976Thr
NM_057166.4:c.7106A>C	NP_476507.3:p.Lys2369Thr
NM_057167.3:c.8309A>C	NP_476508.2:p.Lys2770Thr
XM_005246065.1:c.8327A>C	XP_005246122.1:p.Lys2776Thr
XM_005246066.1:c.7706A>C	XP_005246123.1:p.Lys2569Thr
XM_006712253.1:c.8426A>C	XP_006712316.1:p.Lys2809Thr
XM_011510574.1:c.8924A>C	XP_011508876.1:p.Lys2975Thr
XM_011510575.1:c.6521A>C	XP_011508877.1:p.Lys2174Thr
XM_017003304.1:c.6521A>C	XP_016858793.1:p.Lys2174Thr
XM_024452684.1:c.7706A>C	XP_024308452.1:p.Lys2569Thr
NM_004369.4:c.8927A>C MANE Select	NP_004360.2:p.Lys2976Thr
NM_057166.5:c.7106A>C	NP_476507.3:p.Lys2369Thr
NM_057167.4:c.8309A>C	NP_476508.2:p.Lys2770Thr