Canonical Allele Identifier: CA351216600

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238268765C>G (hg19) ; chr2:g.237360122C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237360122C>G , CM000664.2:g.237360122C>G	GRCh38
NC_000002.11:g.238268765C>G , CM000664.1:g.238268765C>G	GRCh37
NC_000002.10:g.237933504C>G	NCBI36
NG_008676.1:g.59086G>C , LRG_473:g.59086G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.5630G>C	ENSP00000315873.4:p.Gly1877Ala
ENST00000295550.9:c.6248G>C MANE Select	ENSP00000295550.4:p.Gly2083Ala
ENST00000295550.8:c.6248G>C	ENSP00000295550.4:p.Gly2083Ala
ENST00000347401.7:c.4427G>C	ENSP00000315609.4:p.Gly1476Ala
ENST00000353578.8:c.5630G>C	ENSP00000315873.4:p.Gly1877Ala
ENST00000409809.5:c.5630G>C	ENSP00000386844.1:p.Gly1877Ala
ENST00000472056.5:c.4427G>C	ENSP00000418285.1:p.Gly1476Ala
NM_004369.3:c.6248G>C , LRG_473t1:c.6248G>C	NP_004360.2:p.Gly2083Ala
NM_057166.4:c.4427G>C	NP_476507.3:p.Gly1476Ala
NM_057167.3:c.5630G>C	NP_476508.2:p.Gly1877Ala
XM_005246065.1:c.5648G>C	XP_005246122.1:p.Gly1883Ala
XM_005246066.1:c.5027G>C	XP_005246123.1:p.Gly1676Ala
XM_006712253.1:c.5747G>C	XP_006712316.1:p.Gly1916Ala
XM_011510574.1:c.6245G>C	XP_011508876.1:p.Gly2082Ala
XM_011510575.1:c.3842G>C	XP_011508877.1:p.Gly1281Ala
XM_017003304.1:c.3842G>C	XP_016858793.1:p.Gly1281Ala
XM_024452684.1:c.5027G>C	XP_024308452.1:p.Gly1676Ala
NM_004369.4:c.6248G>C MANE Select	NP_004360.2:p.Gly2083Ala
NM_057166.5:c.4427G>C	NP_476507.3:p.Gly1476Ala
NM_057167.4:c.5630G>C	NP_476508.2:p.Gly1877Ala