Canonical Allele Identifier: CA381465628

Gene: CTSF

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66567259A>C , CM000673.2:g.66567259A>C	GRCh38
NC_000011.9:g.66334730A>C , CM000673.1:g.66334730A>C	GRCh37
NC_000011.8:g.66091306A>C	NCBI36
NG_032973.1:g.6318T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003793.4:c.594T>G MANE Select	NP_003784.2:p.Tyr198Ter
ENST00000310325.10:c.594T>G MANE Select	ENSP00000310832.5:p.Tyr198Ter
NM_003793.3:c.594T>G	NP_003784.2:p.Tyr198Ter
ENST00000310325.9:c.594T>G	ENSP00000310832.5:p.Tyr198Ter
ENST00000524994.5:c.139T>G
ENST00000524994.6:c.594T>G	ENSP00000433082.2:p.Tyr198Ter
ENST00000525733.6:c.594T>G	ENSP00000434936.2:p.Tyr198Ter
ENST00000526010.1:c.318T>G	ENSP00000435822.1:p.Tyr106Ter
ENST00000526010.2:c.318T>G	ENSP00000435822.2:p.Tyr106Ter
ENST00000527141.5:n.115T>G
ENST00000527141.6:n.493T>G
ENST00000529561.5:n.432T>G
ENST00000529561.6:n.432T>G
ENST00000530565.6:n.123T>G
ENST00000533168.1:n.449T>G
ENST00000533168.2:n.682T>G
ENST00000676860.1:n.545T>G
ENST00000676924.1:c.594T>G	ENSP00000503579.1:p.Tyr198Ter
ENST00000677005.1:c.594T>G	ENSP00000503238.1:p.Tyr198Ter
ENST00000677186.1:n.714T>G
ENST00000677298.1:n.1000T>G
ENST00000677365.1:n.653T>G
ENST00000677526.1:c.594T>G	ENSP00000504693.1:p.Tyr198Ter
ENST00000677587.1:c.636T>G	ENSP00000503791.1:p.Tyr212Ter
ENST00000677779.1:n.439T>G
ENST00000677896.1:c.585T>G	ENSP00000504605.1:p.Tyr195Ter
ENST00000677920.1:c.594T>G	ENSP00000503614.1:p.Tyr198Ter
ENST00000678154.1:c.*256T>G	ENSP00000502935.1:n.*256T>G
ENST00000678294.1:n.710T>G
ENST00000678305.1:c.522T>G	ENSP00000504383.1:p.Tyr174Ter
ENST00000678383.1:n.603T>G
ENST00000678413.1:c.594T>G	ENSP00000503232.1:p.Tyr198Ter
ENST00000678471.1:c.594T>G	ENSP00000502949.1:p.Tyr198Ter
ENST00000678710.1:c.594T>G	ENSP00000504254.1:p.Tyr198Ter
ENST00000678872.1:c.594T>G	ENSP00000503425.1:p.Tyr198Ter
ENST00000678946.1:n.526T>G
ENST00000678953.1:c.*330T>G	ENSP00000504169.1:n.*330T>G
ENST00000679011.1:c.594T>G	ENSP00000503980.1:p.Tyr198Ter
ENST00000679024.1:c.594T>G	ENSP00000503506.1:p.Tyr198Ter
ENST00000679160.1:c.522T>G	ENSP00000503972.1:p.Tyr174Ter
ENST00000679225.1:n.537T>G
ENST00000679314.1:c.594T>G	ENSP00000503465.1:p.Tyr198Ter
ENST00000679347.1:c.594T>G	ENSP00000503676.1:p.Tyr198Ter
XM_011545328.1:c.414T>G	XP_011543630.1:p.Tyr138Ter
XM_011545328.2:c.414T>G	XP_011543630.1:p.Tyr138Ter