Canonical Allele Identifier: CA1979734341
Gene: CTSF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66565841G= , CM000673.2:g.66565841G= GRCh38
NC_000011.9:g.66333312G= , CM000673.1:g.66333312G= GRCh37
NC_000011.8:g.66089888G= NCBI36
NG_032973.1:g.7736C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310325.10:c.954C= MANE Select ENSP00000310832.5:p.Leu318=
ENST00000524994.6:c.951C= ENSP00000433082.2:p.Leu317=
ENST00000525733.6:c.*148C= ENSP00000434936.2:n.*148C=
ENST00000526010.2:c.678C= ENSP00000435822.2:p.Leu226=
ENST00000527141.6:n.853C=
ENST00000530565.6:n.577C=
ENST00000533168.2:n.1042C=
ENST00000676860.1:n.905C=
ENST00000676924.1:c.954C= ENSP00000503579.1:p.Leu318=
ENST00000677005.1:c.954C= ENSP00000503238.1:p.Leu318=
ENST00000677186.1:n.1074C=
ENST00000677298.1:n.1360C=
ENST00000677365.1:n.1013C=
ENST00000677526.1:c.868-90C= ENSP00000504693.1:n.868-90C=
ENST00000677587.1:c.996C= ENSP00000503791.1:p.Leu332=
ENST00000677779.1:n.799C=
ENST00000677896.1:c.945C= ENSP00000504605.1:p.Leu315=
ENST00000677920.1:c.*206C= ENSP00000503614.1:n.*206C=
ENST00000678154.1:c.*616C= ENSP00000502935.1:n.*616C=
ENST00000678294.1:n.1070C=
ENST00000678305.1:c.882C= ENSP00000504383.1:p.Leu294=
ENST00000678383.1:n.963C=
ENST00000678413.1:c.*148C= ENSP00000503232.1:n.*148C=
ENST00000678471.1:c.954C= ENSP00000502949.1:p.Leu318=
ENST00000678614.1:n.134C=
ENST00000678710.1:c.954C= ENSP00000504254.1:p.Leu318=
ENST00000678872.1:c.954C= ENSP00000503425.1:p.Leu318=
ENST00000678946.1:n.886C=
ENST00000678953.1:c.*690C= ENSP00000504169.1:n.*690C=
ENST00000679011.1:c.868-90C= ENSP00000503980.1:n.868-90C=
ENST00000679024.1:c.954C= ENSP00000503506.1:p.Leu318=
ENST00000679160.1:c.879C= ENSP00000503972.1:p.Leu293=
ENST00000679225.1:n.894C=
ENST00000679314.1:c.954C= ENSP00000503465.1:p.Leu318=
ENST00000679347.1:c.954C= ENSP00000503676.1:p.Leu318=
ENST00000310325.9:c.954C= ENSP00000310832.5:p.Leu318=
ENST00000524994.5:c.496C=
ENST00000525733.5:c.223C=
ENST00000527141.5:n.475C=
ENST00000529199.1:n.214C=
ENST00000530565.5:n.200C=
NM_003793.3:c.954C= NP_003784.2:p.Leu318=
XM_011545328.1:c.774C= XP_011543630.1:p.Leu258=
XM_011545328.2:c.774C= XP_011543630.1:p.Leu258=
NM_003793.4:c.954C= MANE Select NP_003784.2:p.Leu318=