Canonical Allele Identifier: CA431701089

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244887T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336244T>G , CM000664.2:g.237336244T>G	GRCh38
NC_000002.11:g.238244887T>G , CM000664.1:g.238244887T>G	GRCh37
NC_000002.10:g.237909626T>G	NCBI36
NG_008676.1:g.82964A>C , LRG_473:g.82964A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1501A>C
ENST00000353578.9:c.8238A>C	ENSP00000315873.4:p.Val2746=
ENST00000682957.1:c.983A>C
ENST00000684508.1:n.1123A>C
ENST00000295550.9:c.8856A>C MANE Select	ENSP00000295550.4:p.Val2952=
ENST00000295550.8:c.8856A>C	ENSP00000295550.4:p.Val2952=
ENST00000347401.7:c.7032A>C	ENSP00000315609.4:p.Val2344=
ENST00000353578.8:c.8238A>C	ENSP00000315873.4:p.Val2746=
ENST00000409809.5:c.8238A>C	ENSP00000386844.1:p.Val2746=
ENST00000472056.5:c.7035A>C	ENSP00000418285.1:p.Val2345=
ENST00000491769.1:n.5298A>C
NM_004369.3:c.8856A>C , LRG_473t1:c.8856A>C	NP_004360.2:p.Val2952=
NM_057166.4:c.7035A>C	NP_476507.3:p.Val2345=
NM_057167.3:c.8238A>C	NP_476508.2:p.Val2746=
XM_005246065.1:c.8256A>C	XP_005246122.1:p.Val2752=
XM_005246066.1:c.7635A>C	XP_005246123.1:p.Val2545=
XM_006712253.1:c.8355A>C	XP_006712316.1:p.Val2785=
XM_011510574.1:c.8853A>C	XP_011508876.1:p.Val2951=
XM_011510575.1:c.6450A>C	XP_011508877.1:p.Val2150=
XM_017003304.1:c.6450A>C	XP_016858793.1:p.Val2150=
XM_024452684.1:c.7635A>C	XP_024308452.1:p.Val2545=
NM_004369.4:c.8856A>C MANE Select	NP_004360.2:p.Val2952=
NM_057166.5:c.7035A>C	NP_476507.3:p.Val2345=
NM_057167.4:c.8238A>C	NP_476508.2:p.Val2746=