Canonical Allele Identifier: CA351202395

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238253138A>C (hg19) ; chr2:g.237344495A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344495A>C , CM000664.2:g.237344495A>C	GRCh38
NC_000002.11:g.238253138A>C , CM000664.1:g.238253138A>C	GRCh37
NC_000002.10:g.237917877A>C	NCBI36
NG_008676.1:g.74713T>G , LRG_473:g.74713T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.168T>G
ENST00000353578.9:c.6905T>G	ENSP00000315873.4:p.Met2302Arg
ENST00000295550.9:c.7523T>G MANE Select	ENSP00000295550.4:p.Met2508Arg
ENST00000295550.8:c.7523T>G	ENSP00000295550.4:p.Met2508Arg
ENST00000347401.7:c.5699T>G	ENSP00000315609.4:p.Met1900Arg
ENST00000353578.8:c.6905T>G	ENSP00000315873.4:p.Met2302Arg
ENST00000409809.5:c.6905T>G	ENSP00000386844.1:p.Met2302Arg
ENST00000472056.5:c.5702T>G	ENSP00000418285.1:p.Met1901Arg
ENST00000491769.1:n.1777T>G
NM_004369.3:c.7523T>G , LRG_473t1:c.7523T>G	NP_004360.2:p.Met2508Arg
NM_057166.4:c.5702T>G	NP_476507.3:p.Met1901Arg
NM_057167.3:c.6905T>G	NP_476508.2:p.Met2302Arg
XM_005246065.1:c.6923T>G	XP_005246122.1:p.Met2308Arg
XM_005246066.1:c.6302T>G	XP_005246123.1:p.Met2101Arg
XM_006712253.1:c.7022T>G	XP_006712316.1:p.Met2341Arg
XM_011510574.1:c.7520T>G	XP_011508876.1:p.Met2507Arg
XM_011510575.1:c.5117T>G	XP_011508877.1:p.Met1706Arg
XM_017003304.1:c.5117T>G	XP_016858793.1:p.Met1706Arg
XM_024452684.1:c.6302T>G	XP_024308452.1:p.Met2101Arg
NM_004369.4:c.7523T>G MANE Select	NP_004360.2:p.Met2508Arg
NM_057166.5:c.5702T>G	NP_476507.3:p.Met1901Arg
NM_057167.4:c.6905T>G	NP_476508.2:p.Met2302Arg