Canonical Allele Identifier: CA351198860

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238280810A>G (hg19) ; chr2:g.237372167A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237372167A>G , CM000664.2:g.237372167A>G	GRCh38
NC_000002.11:g.238280810A>G , CM000664.1:g.238280810A>G	GRCh37
NC_000002.10:g.237945549A>G	NCBI36
NG_008676.1:g.47041T>C , LRG_473:g.47041T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.3232T>C	ENSP00000315873.4:p.Phe1078Leu
ENST00000295550.9:c.3850T>C MANE Select	ENSP00000295550.4:p.Phe1284Leu
ENST00000295550.8:c.3850T>C	ENSP00000295550.4:p.Phe1284Leu
ENST00000347401.7:c.2029T>C	ENSP00000315609.4:p.Phe677Leu
ENST00000353578.8:c.3232T>C	ENSP00000315873.4:p.Phe1078Leu
ENST00000392003.6:c.2629T>C	ENSP00000375860.2:p.Phe877Leu
ENST00000392004.7:c.3232T>C	ENSP00000375861.3:p.Phe1078Leu
ENST00000409809.5:c.3232T>C	ENSP00000386844.1:p.Phe1078Leu
ENST00000472056.5:c.2029T>C	ENSP00000418285.1:p.Phe677Leu
NM_004369.3:c.3850T>C , LRG_473t1:c.3850T>C	NP_004360.2:p.Phe1284Leu
NM_057164.4:c.2629T>C	NP_476505.3:p.Phe877Leu
NM_057165.4:c.3232T>C	NP_476506.3:p.Phe1078Leu
NM_057166.4:c.2029T>C	NP_476507.3:p.Phe677Leu
NM_057167.3:c.3232T>C	NP_476508.2:p.Phe1078Leu
XM_005246065.1:c.3250T>C	XP_005246122.1:p.Phe1084Leu
XM_005246066.1:c.2629T>C	XP_005246123.1:p.Phe877Leu
XM_006712253.1:c.3850T>C	XP_006712316.1:p.Phe1284Leu
XM_011510574.1:c.3850T>C	XP_011508876.1:p.Phe1284Leu
XM_011510575.1:c.1444T>C	XP_011508877.1:p.Phe482Leu
XM_017003304.1:c.1444T>C	XP_016858793.1:p.Phe482Leu
XM_024452684.1:c.2629T>C	XP_024308452.1:p.Phe877Leu
NM_004369.4:c.3850T>C MANE Select	NP_004360.2:p.Phe1284Leu
NM_057164.5:c.2629T>C	NP_476505.3:p.Phe877Leu
NM_057165.5:c.3232T>C	NP_476506.3:p.Phe1078Leu
NM_057166.5:c.2029T>C	NP_476507.3:p.Phe677Leu
NM_057167.4:c.3232T>C	NP_476508.2:p.Phe1078Leu