Canonical Allele Identifier: CA431700921

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244872A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336229A>T , CM000664.2:g.237336229A>T	GRCh38
NC_000002.11:g.238244872A>T , CM000664.1:g.238244872A>T	GRCh37
NC_000002.10:g.237909611A>T	NCBI36
NG_008676.1:g.82979T>A , LRG_473:g.82979T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1516T>A
ENST00000353578.9:c.8253T>A	ENSP00000315873.4:p.Ala2751=
ENST00000682957.1:c.998T>A
ENST00000684508.1:n.1138T>A
ENST00000295550.9:c.8871T>A MANE Select	ENSP00000295550.4:p.Ala2957=
ENST00000295550.8:c.8871T>A	ENSP00000295550.4:p.Ala2957=
ENST00000347401.7:c.7047T>A	ENSP00000315609.4:p.Ala2349=
ENST00000353578.8:c.8253T>A	ENSP00000315873.4:p.Ala2751=
ENST00000409809.5:c.8253T>A	ENSP00000386844.1:p.Ala2751=
ENST00000472056.5:c.7050T>A	ENSP00000418285.1:p.Ala2350=
ENST00000491769.1:n.5313T>A
NM_004369.3:c.8871T>A , LRG_473t1:c.8871T>A	NP_004360.2:p.Ala2957=
NM_057166.4:c.7050T>A	NP_476507.3:p.Ala2350=
NM_057167.3:c.8253T>A	NP_476508.2:p.Ala2751=
XM_005246065.1:c.8271T>A	XP_005246122.1:p.Ala2757=
XM_005246066.1:c.7650T>A	XP_005246123.1:p.Ala2550=
XM_006712253.1:c.8370T>A	XP_006712316.1:p.Ala2790=
XM_011510574.1:c.8868T>A	XP_011508876.1:p.Ala2956=
XM_011510575.1:c.6465T>A	XP_011508877.1:p.Ala2155=
XM_017003304.1:c.6465T>A	XP_016858793.1:p.Ala2155=
XM_024452684.1:c.7650T>A	XP_024308452.1:p.Ala2550=
NM_004369.4:c.8871T>A MANE Select	NP_004360.2:p.Ala2957=
NM_057166.5:c.7050T>A	NP_476507.3:p.Ala2350=
NM_057167.4:c.8253T>A	NP_476508.2:p.Ala2751=