Canonical Allele Identifier: CA351195088

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238249209A>C (hg19) ; chr2:g.237340566A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237340566A>C , CM000664.2:g.237340566A>C	GRCh38
NC_000002.11:g.238249209A>C , CM000664.1:g.238249209A>C	GRCh37
NC_000002.10:g.237913948A>C	NCBI36
NG_008676.1:g.78642T>G , LRG_473:g.78642T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.995T>G
ENST00000353578.9:c.7732T>G	ENSP00000315873.4:p.Tyr2578Asp
ENST00000682957.1:c.353T>G
ENST00000684508.1:n.617T>G
ENST00000295550.9:c.8350T>G MANE Select	ENSP00000295550.4:p.Tyr2784Asp
ENST00000295550.8:c.8350T>G	ENSP00000295550.4:p.Tyr2784Asp
ENST00000347401.7:c.6526T>G	ENSP00000315609.4:p.Tyr2176Asp
ENST00000353578.8:c.7732T>G	ENSP00000315873.4:p.Tyr2578Asp
ENST00000409809.5:c.7732T>G	ENSP00000386844.1:p.Tyr2578Asp
ENST00000468792.1:n.37T>G
ENST00000472056.5:c.6529T>G	ENSP00000418285.1:p.Tyr2177Asp
ENST00000491769.1:n.4792T>G
NM_004369.3:c.8350T>G , LRG_473t1:c.8350T>G	NP_004360.2:p.Tyr2784Asp
NM_057166.4:c.6529T>G	NP_476507.3:p.Tyr2177Asp
NM_057167.3:c.7732T>G	NP_476508.2:p.Tyr2578Asp
XM_005246065.1:c.7750T>G	XP_005246122.1:p.Tyr2584Asp
XM_005246066.1:c.7129T>G	XP_005246123.1:p.Tyr2377Asp
XM_006712253.1:c.7849T>G	XP_006712316.1:p.Tyr2617Asp
XM_011510574.1:c.8347T>G	XP_011508876.1:p.Tyr2783Asp
XM_011510575.1:c.5944T>G	XP_011508877.1:p.Tyr1982Asp
XM_017003304.1:c.5944T>G	XP_016858793.1:p.Tyr1982Asp
XM_024452684.1:c.7129T>G	XP_024308452.1:p.Tyr2377Asp
NM_004369.4:c.8350T>G MANE Select	NP_004360.2:p.Tyr2784Asp
NM_057166.5:c.6529T>G	NP_476507.3:p.Tyr2177Asp
NM_057167.4:c.7732T>G	NP_476508.2:p.Tyr2578Asp