Canonical Allele Identifier: CA351191421

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244931G>A (hg19) ; chr2:g.237336288G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336288G>A , CM000664.2:g.237336288G>A	GRCh38
NC_000002.11:g.238244931G>A , CM000664.1:g.238244931G>A	GRCh37
NC_000002.10:g.237909670G>A	NCBI36
NG_008676.1:g.82920C>T , LRG_473:g.82920C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1457C>T
ENST00000353578.9:c.8194C>T	ENSP00000315873.4:p.Pro2732Ser
ENST00000682957.1:c.939C>T
ENST00000684508.1:n.1079C>T
ENST00000295550.9:c.8812C>T MANE Select	ENSP00000295550.4:p.Pro2938Ser
ENST00000295550.8:c.8812C>T	ENSP00000295550.4:p.Pro2938Ser
ENST00000347401.7:c.6988C>T	ENSP00000315609.4:p.Pro2330Ser
ENST00000353578.8:c.8194C>T	ENSP00000315873.4:p.Pro2732Ser
ENST00000409809.5:c.8194C>T	ENSP00000386844.1:p.Pro2732Ser
ENST00000472056.5:c.6991C>T	ENSP00000418285.1:p.Pro2331Ser
ENST00000491769.1:n.5254C>T
NM_004369.3:c.8812C>T , LRG_473t1:c.8812C>T	NP_004360.2:p.Pro2938Ser
NM_057166.4:c.6991C>T	NP_476507.3:p.Pro2331Ser
NM_057167.3:c.8194C>T	NP_476508.2:p.Pro2732Ser
XM_005246065.1:c.8212C>T	XP_005246122.1:p.Pro2738Ser
XM_005246066.1:c.7591C>T	XP_005246123.1:p.Pro2531Ser
XM_006712253.1:c.8311C>T	XP_006712316.1:p.Pro2771Ser
XM_011510574.1:c.8809C>T	XP_011508876.1:p.Pro2937Ser
XM_011510575.1:c.6406C>T	XP_011508877.1:p.Pro2136Ser
XM_017003304.1:c.6406C>T	XP_016858793.1:p.Pro2136Ser
XM_024452684.1:c.7591C>T	XP_024308452.1:p.Pro2531Ser
NM_004369.4:c.8812C>T MANE Select	NP_004360.2:p.Pro2938Ser
NM_057166.5:c.6991C>T	NP_476507.3:p.Pro2331Ser
NM_057167.4:c.8194C>T	NP_476508.2:p.Pro2732Ser