Canonical Allele Identifier: CA351194438

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238249124A>G (hg19) ; chr2:g.237340481A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237340481A>G , CM000664.2:g.237340481A>G	GRCh38
NC_000002.11:g.238249124A>G , CM000664.1:g.238249124A>G	GRCh37
NC_000002.10:g.237913863A>G	NCBI36
NG_008676.1:g.78727T>C , LRG_473:g.78727T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1080T>C
ENST00000353578.9:c.7817T>C	ENSP00000315873.4:p.Phe2606Ser
ENST00000682957.1:c.438T>C
ENST00000684508.1:n.702T>C
ENST00000295550.9:c.8435T>C MANE Select	ENSP00000295550.4:p.Phe2812Ser
ENST00000295550.8:c.8435T>C	ENSP00000295550.4:p.Phe2812Ser
ENST00000347401.7:c.6611T>C	ENSP00000315609.4:p.Phe2204Ser
ENST00000353578.8:c.7817T>C	ENSP00000315873.4:p.Phe2606Ser
ENST00000409809.5:c.7817T>C	ENSP00000386844.1:p.Phe2606Ser
ENST00000468792.1:n.122T>C
ENST00000472056.5:c.6614T>C	ENSP00000418285.1:p.Phe2205Ser
ENST00000491769.1:n.4877T>C
NM_004369.3:c.8435T>C , LRG_473t1:c.8435T>C	NP_004360.2:p.Phe2812Ser
NM_057166.4:c.6614T>C	NP_476507.3:p.Phe2205Ser
NM_057167.3:c.7817T>C	NP_476508.2:p.Phe2606Ser
XM_005246065.1:c.7835T>C	XP_005246122.1:p.Phe2612Ser
XM_005246066.1:c.7214T>C	XP_005246123.1:p.Phe2405Ser
XM_006712253.1:c.7934T>C	XP_006712316.1:p.Phe2645Ser
XM_011510574.1:c.8432T>C	XP_011508876.1:p.Phe2811Ser
XM_011510575.1:c.6029T>C	XP_011508877.1:p.Phe2010Ser
XM_017003304.1:c.6029T>C	XP_016858793.1:p.Phe2010Ser
XM_024452684.1:c.7214T>C	XP_024308452.1:p.Phe2405Ser
NM_004369.4:c.8435T>C MANE Select	NP_004360.2:p.Phe2812Ser
NM_057166.5:c.6614T>C	NP_476507.3:p.Phe2205Ser
NM_057167.4:c.7817T>C	NP_476508.2:p.Phe2606Ser