Canonical Allele Identifier: CA475371051

Gene: CTSF

Linked Data

• MyVariant Identifiers: chr11:g.66333212G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66565741G>A , CM000673.2:g.66565741G>A	GRCh38
NC_000011.9:g.66333212G>A , CM000673.1:g.66333212G>A	GRCh37
NC_000011.8:g.66089788G>A	NCBI36
NG_032973.1:g.7836C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310325.10:c.975C>T MANE Select	ENSP00000310832.5:p.Asp325=
ENST00000524994.6:c.972C>T	ENSP00000433082.2:p.Asp324=
ENST00000525733.6:c.*169C>T	ENSP00000434936.2:n.*169C>T
ENST00000526010.2:c.699C>T	ENSP00000435822.2:p.Asp233=
ENST00000527141.6:n.874C>T
ENST00000530565.6:n.677C>T
ENST00000533168.2:n.1063C>T
ENST00000676860.1:n.926C>T
ENST00000676924.1:c.973C>T	ENSP00000503579.1:p.Leu325=
ENST00000677005.1:c.975C>T	ENSP00000503238.1:p.Asp325=
ENST00000677186.1:n.1095C>T
ENST00000677298.1:n.1381C>T
ENST00000677365.1:n.1113C>T
ENST00000677526.1:c.878C>T	ENSP00000504693.1:p.Thr293Ile
ENST00000677587.1:c.1017C>T	ENSP00000503791.1:p.Asp339=
ENST00000677779.1:n.820C>T
ENST00000677896.1:c.966C>T	ENSP00000504605.1:p.Asp322=
ENST00000677920.1:c.*227C>T	ENSP00000503614.1:n.*227C>T
ENST00000678154.1:c.*637C>T	ENSP00000502935.1:n.*637C>T
ENST00000678294.1:n.1091C>T
ENST00000678305.1:c.903C>T	ENSP00000504383.1:p.Asp301=
ENST00000678383.1:n.1063C>T
ENST00000678413.1:c.*169C>T	ENSP00000503232.1:n.*169C>T
ENST00000678471.1:c.975C>T	ENSP00000502949.1:p.Asp325=
ENST00000678614.1:n.234C>T
ENST00000678710.1:c.975C>T	ENSP00000504254.1:p.Asp325=
ENST00000678872.1:c.975C>T	ENSP00000503425.1:p.Asp325=
ENST00000678946.1:n.907C>T
ENST00000678953.1:c.*711C>T	ENSP00000504169.1:n.*711C>T
ENST00000679011.1:c.878C>T	ENSP00000503980.1:p.Thr293Ile
ENST00000679024.1:c.975C>T	ENSP00000503506.1:p.Asp325=
ENST00000679160.1:c.900C>T	ENSP00000503972.1:p.Asp300=
ENST00000679225.1:n.915C>T
ENST00000679314.1:c.975C>T	ENSP00000503465.1:p.Asp325=
ENST00000679347.1:c.975C>T	ENSP00000503676.1:p.Asp325=
ENST00000310325.9:c.975C>T	ENSP00000310832.5:p.Asp325=
ENST00000524994.5:c.517C>T
ENST00000525733.5:c.242C>T
ENST00000527141.5:n.496C>T
ENST00000529199.1:n.314C>T
ENST00000530565.5:n.300C>T
NM_003793.3:c.975C>T	NP_003784.2:p.Asp325=
XM_011545328.1:c.795C>T	XP_011543630.1:p.Asp265=
XM_011545328.2:c.795C>T	XP_011543630.1:p.Asp265=
NM_003793.4:c.975C>T MANE Select	NP_003784.2:p.Asp325=