Canonical Allele Identifier: CA431674950

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238245175T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336532T>G , CM000664.2:g.237336532T>G	GRCh38
NC_000002.11:g.238245175T>G , CM000664.1:g.238245175T>G	GRCh37
NC_000002.10:g.237909914T>G	NCBI36
NG_008676.1:g.82676A>C , LRG_473:g.82676A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1213A>C
ENST00000353578.9:c.7950A>C	ENSP00000315873.4:p.Val2650=
ENST00000682957.1:c.695A>C
ENST00000684508.1:n.835A>C
ENST00000295550.9:c.8568A>C MANE Select	ENSP00000295550.4:p.Val2856=
ENST00000295550.8:c.8568A>C	ENSP00000295550.4:p.Val2856=
ENST00000347401.7:c.6744A>C	ENSP00000315609.4:p.Val2248=
ENST00000353578.8:c.7950A>C	ENSP00000315873.4:p.Val2650=
ENST00000409809.5:c.7950A>C	ENSP00000386844.1:p.Val2650=
ENST00000472056.5:c.6747A>C	ENSP00000418285.1:p.Val2249=
ENST00000491769.1:n.5010A>C
NM_004369.3:c.8568A>C , LRG_473t1:c.8568A>C	NP_004360.2:p.Val2856=
NM_057166.4:c.6747A>C	NP_476507.3:p.Val2249=
NM_057167.3:c.7950A>C	NP_476508.2:p.Val2650=
XM_005246065.1:c.7968A>C	XP_005246122.1:p.Val2656=
XM_005246066.1:c.7347A>C	XP_005246123.1:p.Val2449=
XM_006712253.1:c.8067A>C	XP_006712316.1:p.Val2689=
XM_011510574.1:c.8565A>C	XP_011508876.1:p.Val2855=
XM_011510575.1:c.6162A>C	XP_011508877.1:p.Val2054=
XM_017003304.1:c.6162A>C	XP_016858793.1:p.Val2054=
XM_024452684.1:c.7347A>C	XP_024308452.1:p.Val2449=
NM_004369.4:c.8568A>C MANE Select	NP_004360.2:p.Val2856=
NM_057166.5:c.6747A>C	NP_476507.3:p.Val2249=
NM_057167.4:c.7950A>C	NP_476508.2:p.Val2650=