Canonical Allele Identifier: CA351202098

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238253093G>C (hg19) ; chr2:g.237344450G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344450G>C , CM000664.2:g.237344450G>C	GRCh38
NC_000002.11:g.238253093G>C , CM000664.1:g.238253093G>C	GRCh37
NC_000002.10:g.237917832G>C	NCBI36
NG_008676.1:g.74758C>G , LRG_473:g.74758C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.213C>G
ENST00000353578.9:c.6950C>G	ENSP00000315873.4:p.Ser2317Cys
ENST00000295550.9:c.7568C>G MANE Select	ENSP00000295550.4:p.Ser2523Cys
ENST00000295550.8:c.7568C>G	ENSP00000295550.4:p.Ser2523Cys
ENST00000347401.7:c.5744C>G	ENSP00000315609.4:p.Ser1915Cys
ENST00000353578.8:c.6950C>G	ENSP00000315873.4:p.Ser2317Cys
ENST00000409809.5:c.6950C>G	ENSP00000386844.1:p.Ser2317Cys
ENST00000472056.5:c.5747C>G	ENSP00000418285.1:p.Ser1916Cys
ENST00000491769.1:n.1822C>G
NM_004369.3:c.7568C>G , LRG_473t1:c.7568C>G	NP_004360.2:p.Ser2523Cys
NM_057166.4:c.5747C>G	NP_476507.3:p.Ser1916Cys
NM_057167.3:c.6950C>G	NP_476508.2:p.Ser2317Cys
XM_005246065.1:c.6968C>G	XP_005246122.1:p.Ser2323Cys
XM_005246066.1:c.6347C>G	XP_005246123.1:p.Ser2116Cys
XM_006712253.1:c.7067C>G	XP_006712316.1:p.Ser2356Cys
XM_011510574.1:c.7565C>G	XP_011508876.1:p.Ser2522Cys
XM_011510575.1:c.5162C>G	XP_011508877.1:p.Ser1721Cys
XM_017003304.1:c.5162C>G	XP_016858793.1:p.Ser1721Cys
XM_024452684.1:c.6347C>G	XP_024308452.1:p.Ser2116Cys
NM_004369.4:c.7568C>G MANE Select	NP_004360.2:p.Ser2523Cys
NM_057166.5:c.5747C>G	NP_476507.3:p.Ser1916Cys
NM_057167.4:c.6950C>G	NP_476508.2:p.Ser2317Cys