Canonical Allele Identifier: CA351191745

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238245006C>G (hg19) ; chr2:g.237336363C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336363C>G , CM000664.2:g.237336363C>G	GRCh38
NC_000002.11:g.238245006C>G , CM000664.1:g.238245006C>G	GRCh37
NC_000002.10:g.237909745C>G	NCBI36
NG_008676.1:g.82845G>C , LRG_473:g.82845G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1382G>C
ENST00000353578.9:c.8119G>C	ENSP00000315873.4:p.Ala2707Pro
ENST00000682957.1:c.864G>C
ENST00000684508.1:n.1004G>C
ENST00000295550.9:c.8737G>C MANE Select	ENSP00000295550.4:p.Ala2913Pro
ENST00000295550.8:c.8737G>C	ENSP00000295550.4:p.Ala2913Pro
ENST00000347401.7:c.6913G>C	ENSP00000315609.4:p.Ala2305Pro
ENST00000353578.8:c.8119G>C	ENSP00000315873.4:p.Ala2707Pro
ENST00000409809.5:c.8119G>C	ENSP00000386844.1:p.Ala2707Pro
ENST00000472056.5:c.6916G>C	ENSP00000418285.1:p.Ala2306Pro
ENST00000491769.1:n.5179G>C
NM_004369.3:c.8737G>C , LRG_473t1:c.8737G>C	NP_004360.2:p.Ala2913Pro
NM_057166.4:c.6916G>C	NP_476507.3:p.Ala2306Pro
NM_057167.3:c.8119G>C	NP_476508.2:p.Ala2707Pro
XM_005246065.1:c.8137G>C	XP_005246122.1:p.Ala2713Pro
XM_005246066.1:c.7516G>C	XP_005246123.1:p.Ala2506Pro
XM_006712253.1:c.8236G>C	XP_006712316.1:p.Ala2746Pro
XM_011510574.1:c.8734G>C	XP_011508876.1:p.Ala2912Pro
XM_011510575.1:c.6331G>C	XP_011508877.1:p.Ala2111Pro
XM_017003304.1:c.6331G>C	XP_016858793.1:p.Ala2111Pro
XM_024452684.1:c.7516G>C	XP_024308452.1:p.Ala2506Pro
NM_004369.4:c.8737G>C MANE Select	NP_004360.2:p.Ala2913Pro
NM_057166.5:c.6916G>C	NP_476507.3:p.Ala2306Pro
NM_057167.4:c.8119G>C	NP_476508.2:p.Ala2707Pro