Canonical Allele Identifier: CA351191930

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238245100C>A (hg19) ; chr2:g.237336457C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336457C>A , CM000664.2:g.237336457C>A	GRCh38
NC_000002.11:g.238245100C>A , CM000664.1:g.238245100C>A	GRCh37
NC_000002.10:g.237909839C>A	NCBI36
NG_008676.1:g.82751G>T , LRG_473:g.82751G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1288G>T
ENST00000353578.9:c.8025G>T	ENSP00000315873.4:p.Lys2675Asn
ENST00000682957.1:c.770G>T
ENST00000684508.1:n.910G>T
ENST00000295550.9:c.8643G>T MANE Select	ENSP00000295550.4:p.Lys2881Asn
ENST00000295550.8:c.8643G>T	ENSP00000295550.4:p.Lys2881Asn
ENST00000347401.7:c.6819G>T	ENSP00000315609.4:p.Lys2273Asn
ENST00000353578.8:c.8025G>T	ENSP00000315873.4:p.Lys2675Asn
ENST00000409809.5:c.8025G>T	ENSP00000386844.1:p.Lys2675Asn
ENST00000472056.5:c.6822G>T	ENSP00000418285.1:p.Lys2274Asn
ENST00000491769.1:n.5085G>T
NM_004369.3:c.8643G>T , LRG_473t1:c.8643G>T	NP_004360.2:p.Lys2881Asn
NM_057166.4:c.6822G>T	NP_476507.3:p.Lys2274Asn
NM_057167.3:c.8025G>T	NP_476508.2:p.Lys2675Asn
XM_005246065.1:c.8043G>T	XP_005246122.1:p.Lys2681Asn
XM_005246066.1:c.7422G>T	XP_005246123.1:p.Lys2474Asn
XM_006712253.1:c.8142G>T	XP_006712316.1:p.Lys2714Asn
XM_011510574.1:c.8640G>T	XP_011508876.1:p.Lys2880Asn
XM_011510575.1:c.6237G>T	XP_011508877.1:p.Lys2079Asn
XM_017003304.1:c.6237G>T	XP_016858793.1:p.Lys2079Asn
XM_024452684.1:c.7422G>T	XP_024308452.1:p.Lys2474Asn
NM_004369.4:c.8643G>T MANE Select	NP_004360.2:p.Lys2881Asn
NM_057166.5:c.6822G>T	NP_476507.3:p.Lys2274Asn
NM_057167.4:c.8025G>T	NP_476508.2:p.Lys2675Asn