Canonical Allele Identifier: CA351195786

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238249308G>A (hg19) ; chr2:g.237340665G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237340665G>A , CM000664.2:g.237340665G>A	GRCh38
NC_000002.11:g.238249308G>A , CM000664.1:g.238249308G>A	GRCh37
NC_000002.10:g.237914047G>A	NCBI36
NG_008676.1:g.78543C>T , LRG_473:g.78543C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.896C>T
ENST00000353578.9:c.7633C>T	ENSP00000315873.4:p.Gln2545Ter
ENST00000682957.1:c.254C>T
ENST00000684508.1:n.518C>T
ENST00000295550.9:c.8251C>T MANE Select	ENSP00000295550.4:p.Gln2751Ter
ENST00000295550.8:c.8251C>T	ENSP00000295550.4:p.Gln2751Ter
ENST00000347401.7:c.6427C>T	ENSP00000315609.4:p.Gln2143Ter
ENST00000353578.8:c.7633C>T	ENSP00000315873.4:p.Gln2545Ter
ENST00000409809.5:c.7633C>T	ENSP00000386844.1:p.Gln2545Ter
ENST00000472056.5:c.6430C>T	ENSP00000418285.1:p.Gln2144Ter
ENST00000491769.1:n.4693C>T
NM_004369.3:c.8251C>T , LRG_473t1:c.8251C>T	NP_004360.2:p.Gln2751Ter
NM_057166.4:c.6430C>T	NP_476507.3:p.Gln2144Ter
NM_057167.3:c.7633C>T	NP_476508.2:p.Gln2545Ter
XM_005246065.1:c.7651C>T	XP_005246122.1:p.Gln2551Ter
XM_005246066.1:c.7030C>T	XP_005246123.1:p.Gln2344Ter
XM_006712253.1:c.7750C>T	XP_006712316.1:p.Gln2584Ter
XM_011510574.1:c.8248C>T	XP_011508876.1:p.Gln2750Ter
XM_011510575.1:c.5845C>T	XP_011508877.1:p.Gln1949Ter
XM_017003304.1:c.5845C>T	XP_016858793.1:p.Gln1949Ter
XM_024452684.1:c.7030C>T	XP_024308452.1:p.Gln2344Ter
NM_004369.4:c.8251C>T MANE Select	NP_004360.2:p.Gln2751Ter
NM_057166.5:c.6430C>T	NP_476507.3:p.Gln2144Ter
NM_057167.4:c.7633C>T	NP_476508.2:p.Gln2545Ter