Canonical Allele Identifier: CA351188429

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238275685T>A (hg19) ; chr2:g.237367042T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237367042T>A , CM000664.2:g.237367042T>A	GRCh38
NC_000002.11:g.238275685T>A , CM000664.1:g.238275685T>A	GRCh37
NC_000002.10:g.237940424T>A	NCBI36
NG_008676.1:g.52166A>T , LRG_473:g.52166A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000353578.9:c.4527A>T	ENSP00000315873.4:p.Arg1509Ser
ENST00000295550.9:c.5145A>T MANE Select	ENSP00000295550.4:p.Arg1715Ser
ENST00000295550.8:c.5145A>T	ENSP00000295550.4:p.Arg1715Ser
ENST00000347401.7:c.3324A>T	ENSP00000315609.4:p.Arg1108Ser
ENST00000353578.8:c.4527A>T	ENSP00000315873.4:p.Arg1509Ser
ENST00000409809.5:c.4527A>T	ENSP00000386844.1:p.Arg1509Ser
ENST00000472056.5:c.3324A>T	ENSP00000418285.1:p.Arg1108Ser
NM_004369.3:c.5145A>T , LRG_473t1:c.5145A>T	NP_004360.2:p.Arg1715Ser
NM_057166.4:c.3324A>T	NP_476507.3:p.Arg1108Ser
NM_057167.3:c.4527A>T	NP_476508.2:p.Arg1509Ser
XM_005246065.1:c.4545A>T	XP_005246122.1:p.Arg1515Ser
XM_005246066.1:c.3924A>T	XP_005246123.1:p.Arg1308Ser
XM_006712253.1:c.4644A>T	XP_006712316.1:p.Arg1548Ser
XM_011510574.1:c.5142A>T	XP_011508876.1:p.Arg1714Ser
XM_011510575.1:c.2739A>T	XP_011508877.1:p.Arg913Ser
XM_017003304.1:c.2739A>T	XP_016858793.1:p.Arg913Ser
XM_024452684.1:c.3924A>T	XP_024308452.1:p.Arg1308Ser
NM_004369.4:c.5145A>T MANE Select	NP_004360.2:p.Arg1715Ser
NM_057166.5:c.3324A>T	NP_476507.3:p.Arg1108Ser
NM_057167.4:c.4527A>T	NP_476508.2:p.Arg1509Ser