Canonical Allele Identifier: CA351191138

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244849G>T (hg19) ; chr2:g.237336206G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336206G>T , CM000664.2:g.237336206G>T	GRCh38
NC_000002.11:g.238244849G>T , CM000664.1:g.238244849G>T	GRCh37
NC_000002.10:g.237909588G>T	NCBI36
NG_008676.1:g.83002C>A , LRG_473:g.83002C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1539C>A
ENST00000353578.9:c.8276C>A	ENSP00000315873.4:p.Thr2759Asn
ENST00000682957.1:c.1021C>A
ENST00000684508.1:n.1161C>A
ENST00000295550.9:c.8894C>A MANE Select	ENSP00000295550.4:p.Thr2965Asn
ENST00000295550.8:c.8894C>A	ENSP00000295550.4:p.Thr2965Asn
ENST00000347401.7:c.7070C>A	ENSP00000315609.4:p.Thr2357Asn
ENST00000353578.8:c.8276C>A	ENSP00000315873.4:p.Thr2759Asn
ENST00000409809.5:c.8276C>A	ENSP00000386844.1:p.Thr2759Asn
ENST00000472056.5:c.7073C>A	ENSP00000418285.1:p.Thr2358Asn
ENST00000491769.1:n.5336C>A
NM_004369.3:c.8894C>A , LRG_473t1:c.8894C>A	NP_004360.2:p.Thr2965Asn
NM_057166.4:c.7073C>A	NP_476507.3:p.Thr2358Asn
NM_057167.3:c.8276C>A	NP_476508.2:p.Thr2759Asn
XM_005246065.1:c.8294C>A	XP_005246122.1:p.Thr2765Asn
XM_005246066.1:c.7673C>A	XP_005246123.1:p.Thr2558Asn
XM_006712253.1:c.8393C>A	XP_006712316.1:p.Thr2798Asn
XM_011510574.1:c.8891C>A	XP_011508876.1:p.Thr2964Asn
XM_011510575.1:c.6488C>A	XP_011508877.1:p.Thr2163Asn
XM_017003304.1:c.6488C>A	XP_016858793.1:p.Thr2163Asn
XM_024452684.1:c.7673C>A	XP_024308452.1:p.Thr2558Asn
NM_004369.4:c.8894C>A MANE Select	NP_004360.2:p.Thr2965Asn
NM_057166.5:c.7073C>A	NP_476507.3:p.Thr2358Asn
NM_057167.4:c.8276C>A	NP_476508.2:p.Thr2759Asn