Canonical Allele Identifier: CA381460273

Gene: CTSF

Linked Data

• MyVariant Identifiers: chr11:g.66333206G>T (hg19) ; chr11:g.66565735G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66565735G>T , CM000673.2:g.66565735G>T	GRCh38
NC_000011.9:g.66333206G>T , CM000673.1:g.66333206G>T	GRCh37
NC_000011.8:g.66089782G>T	NCBI36
NG_032973.1:g.7842C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310325.10:c.981C>A MANE Select	ENSP00000310832.5:p.Asp327Glu
ENST00000524994.6:c.978C>A	ENSP00000433082.2:p.Asp326Glu
ENST00000525733.6:c.*175C>A	ENSP00000434936.2:n.*175C>A
ENST00000526010.2:c.705C>A	ENSP00000435822.2:p.Asp235Glu
ENST00000527141.6:n.880C>A
ENST00000530565.6:n.683C>A
ENST00000533168.2:n.1069C>A
ENST00000676860.1:n.932C>A
ENST00000676924.1:c.*1C>A	ENSP00000503579.1:n.*1C>A
ENST00000677005.1:c.981C>A	ENSP00000503238.1:p.Asp327Glu
ENST00000677186.1:n.1101C>A
ENST00000677298.1:n.1387C>A
ENST00000677365.1:n.1119C>A
ENST00000677526.1:c.884C>A	ENSP00000504693.1:p.Thr295Lys
ENST00000677587.1:c.1023C>A	ENSP00000503791.1:p.Asp341Glu
ENST00000677779.1:n.826C>A
ENST00000677896.1:c.972C>A	ENSP00000504605.1:p.Asp324Glu
ENST00000677920.1:c.*233C>A	ENSP00000503614.1:n.*233C>A
ENST00000678154.1:c.*643C>A	ENSP00000502935.1:n.*643C>A
ENST00000678294.1:n.1097C>A
ENST00000678305.1:c.909C>A	ENSP00000504383.1:p.Asp303Glu
ENST00000678383.1:n.1069C>A
ENST00000678413.1:c.*175C>A	ENSP00000503232.1:n.*175C>A
ENST00000678471.1:c.981C>A	ENSP00000502949.1:p.Asp327Glu
ENST00000678614.1:n.240C>A
ENST00000678710.1:c.981C>A	ENSP00000504254.1:p.Asp327Glu
ENST00000678872.1:c.981C>A	ENSP00000503425.1:p.Asp327Glu
ENST00000678946.1:n.913C>A
ENST00000678953.1:c.*717C>A	ENSP00000504169.1:n.*717C>A
ENST00000679011.1:c.884C>A	ENSP00000503980.1:p.Thr295Lys
ENST00000679024.1:c.981C>A	ENSP00000503506.1:p.Asp327Glu
ENST00000679160.1:c.906C>A	ENSP00000503972.1:p.Asp302Glu
ENST00000679225.1:n.921C>A
ENST00000679314.1:c.981C>A	ENSP00000503465.1:p.Asp327Glu
ENST00000679347.1:c.981C>A	ENSP00000503676.1:p.Asp327Glu
ENST00000310325.9:c.981C>A	ENSP00000310832.5:p.Asp327Glu
ENST00000524994.5:c.523C>A
ENST00000525733.5:c.248C>A
ENST00000527141.5:n.502C>A
ENST00000529199.1:n.320C>A
ENST00000530565.5:n.306C>A
NM_003793.3:c.981C>A	NP_003784.2:p.Asp327Glu
XM_011545328.1:c.801C>A	XP_011543630.1:p.Asp267Glu
XM_011545328.2:c.801C>A	XP_011543630.1:p.Asp267Glu
NM_003793.4:c.981C>A MANE Select	NP_003784.2:p.Asp327Glu