Canonical Allele Identifier: CA351195740

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238249300C>G (hg19) ; chr2:g.237340657C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237340657C>G , CM000664.2:g.237340657C>G	GRCh38
NC_000002.11:g.238249300C>G , CM000664.1:g.238249300C>G	GRCh37
NC_000002.10:g.237914039C>G	NCBI36
NG_008676.1:g.78551G>C , LRG_473:g.78551G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.904G>C
ENST00000353578.9:c.7641G>C	ENSP00000315873.4:p.Glu2547Asp
ENST00000682957.1:c.262G>C
ENST00000684508.1:n.526G>C
ENST00000295550.9:c.8259G>C MANE Select	ENSP00000295550.4:p.Glu2753Asp
ENST00000295550.8:c.8259G>C	ENSP00000295550.4:p.Glu2753Asp
ENST00000347401.7:c.6435G>C	ENSP00000315609.4:p.Glu2145Asp
ENST00000353578.8:c.7641G>C	ENSP00000315873.4:p.Glu2547Asp
ENST00000409809.5:c.7641G>C	ENSP00000386844.1:p.Glu2547Asp
ENST00000472056.5:c.6438G>C	ENSP00000418285.1:p.Glu2146Asp
ENST00000491769.1:n.4701G>C
NM_004369.3:c.8259G>C , LRG_473t1:c.8259G>C	NP_004360.2:p.Glu2753Asp
NM_057166.4:c.6438G>C	NP_476507.3:p.Glu2146Asp
NM_057167.3:c.7641G>C	NP_476508.2:p.Glu2547Asp
XM_005246065.1:c.7659G>C	XP_005246122.1:p.Glu2553Asp
XM_005246066.1:c.7038G>C	XP_005246123.1:p.Glu2346Asp
XM_006712253.1:c.7758G>C	XP_006712316.1:p.Glu2586Asp
XM_011510574.1:c.8256G>C	XP_011508876.1:p.Glu2752Asp
XM_011510575.1:c.5853G>C	XP_011508877.1:p.Glu1951Asp
XM_017003304.1:c.5853G>C	XP_016858793.1:p.Glu1951Asp
XM_024452684.1:c.7038G>C	XP_024308452.1:p.Glu2346Asp
NM_004369.4:c.8259G>C MANE Select	NP_004360.2:p.Glu2753Asp
NM_057166.5:c.6438G>C	NP_476507.3:p.Glu2146Asp
NM_057167.4:c.7641G>C	NP_476508.2:p.Glu2547Asp