Canonical Allele Identifier: CA381460297

Gene: CTSF

Linked Data

• MyVariant Identifiers: chr11:g.66333209A>C (hg19) ; chr11:g.66565738A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66565738A>C , CM000673.2:g.66565738A>C	GRCh38
NC_000011.9:g.66333209A>C , CM000673.1:g.66333209A>C	GRCh37
NC_000011.8:g.66089785A>C	NCBI36
NG_032973.1:g.7839T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310325.10:c.978T>G MANE Select	ENSP00000310832.5:p.Cys326Trp
ENST00000524994.6:c.975T>G	ENSP00000433082.2:p.Cys325Trp
ENST00000525733.6:c.*172T>G	ENSP00000434936.2:n.*172T>G
ENST00000526010.2:c.702T>G	ENSP00000435822.2:p.Cys234Trp
ENST00000527141.6:n.877T>G
ENST00000530565.6:n.680T>G
ENST00000533168.2:n.1066T>G
ENST00000676860.1:n.929T>G
ENST00000676924.1:c.976T>G	ENSP00000503579.1:p.Ter326Gly
ENST00000677005.1:c.978T>G	ENSP00000503238.1:p.Cys326Trp
ENST00000677186.1:n.1098T>G
ENST00000677298.1:n.1384T>G
ENST00000677365.1:n.1116T>G
ENST00000677526.1:c.881T>G	ENSP00000504693.1:p.Val294Gly
ENST00000677587.1:c.1020T>G	ENSP00000503791.1:p.Cys340Trp
ENST00000677779.1:n.823T>G
ENST00000677896.1:c.969T>G	ENSP00000504605.1:p.Cys323Trp
ENST00000677920.1:c.*230T>G	ENSP00000503614.1:n.*230T>G
ENST00000678154.1:c.*640T>G	ENSP00000502935.1:n.*640T>G
ENST00000678294.1:n.1094T>G
ENST00000678305.1:c.906T>G	ENSP00000504383.1:p.Cys302Trp
ENST00000678383.1:n.1066T>G
ENST00000678413.1:c.*172T>G	ENSP00000503232.1:n.*172T>G
ENST00000678471.1:c.978T>G	ENSP00000502949.1:p.Cys326Trp
ENST00000678614.1:n.237T>G
ENST00000678710.1:c.978T>G	ENSP00000504254.1:p.Cys326Trp
ENST00000678872.1:c.978T>G	ENSP00000503425.1:p.Cys326Trp
ENST00000678946.1:n.910T>G
ENST00000678953.1:c.*714T>G	ENSP00000504169.1:n.*714T>G
ENST00000679011.1:c.881T>G	ENSP00000503980.1:p.Val294Gly
ENST00000679024.1:c.978T>G	ENSP00000503506.1:p.Cys326Trp
ENST00000679160.1:c.903T>G	ENSP00000503972.1:p.Cys301Trp
ENST00000679225.1:n.918T>G
ENST00000679314.1:c.978T>G	ENSP00000503465.1:p.Cys326Trp
ENST00000679347.1:c.978T>G	ENSP00000503676.1:p.Cys326Trp
ENST00000310325.9:c.978T>G	ENSP00000310832.5:p.Cys326Trp
ENST00000524994.5:c.520T>G
ENST00000525733.5:c.245T>G
ENST00000527141.5:n.499T>G
ENST00000529199.1:n.317T>G
ENST00000530565.5:n.303T>G
NM_003793.3:c.978T>G	NP_003784.2:p.Cys326Trp
XM_011545328.1:c.798T>G	XP_011543630.1:p.Cys266Trp
XM_011545328.2:c.798T>G	XP_011543630.1:p.Cys266Trp
NM_003793.4:c.978T>G MANE Select	NP_003784.2:p.Cys326Trp