Canonical Allele Identifier: CA381460300

Gene: CTSF

Linked Data

• MyVariant Identifiers: chr11:g.66333210C>A (hg19) ; chr11:g.66565739C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66565739C>A , CM000673.2:g.66565739C>A	GRCh38
NC_000011.9:g.66333210C>A , CM000673.1:g.66333210C>A	GRCh37
NC_000011.8:g.66089786C>A	NCBI36
NG_032973.1:g.7838G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310325.10:c.977G>T MANE Select	ENSP00000310832.5:p.Cys326Phe
ENST00000524994.6:c.974G>T	ENSP00000433082.2:p.Cys325Phe
ENST00000525733.6:c.*171G>T	ENSP00000434936.2:n.*171G>T
ENST00000526010.2:c.701G>T	ENSP00000435822.2:p.Cys234Phe
ENST00000527141.6:n.876G>T
ENST00000530565.6:n.679G>T
ENST00000533168.2:n.1065G>T
ENST00000676860.1:n.928G>T
ENST00000676924.1:c.975G>T	ENSP00000503579.1:p.Leu325=
ENST00000677005.1:c.977G>T	ENSP00000503238.1:p.Cys326Phe
ENST00000677186.1:n.1097G>T
ENST00000677298.1:n.1383G>T
ENST00000677365.1:n.1115G>T
ENST00000677526.1:c.880G>T	ENSP00000504693.1:p.Val294Leu
ENST00000677587.1:c.1019G>T	ENSP00000503791.1:p.Cys340Phe
ENST00000677779.1:n.822G>T
ENST00000677896.1:c.968G>T	ENSP00000504605.1:p.Cys323Phe
ENST00000677920.1:c.*229G>T	ENSP00000503614.1:n.*229G>T
ENST00000678154.1:c.*639G>T	ENSP00000502935.1:n.*639G>T
ENST00000678294.1:n.1093G>T
ENST00000678305.1:c.905G>T	ENSP00000504383.1:p.Cys302Phe
ENST00000678383.1:n.1065G>T
ENST00000678413.1:c.*171G>T	ENSP00000503232.1:n.*171G>T
ENST00000678471.1:c.977G>T	ENSP00000502949.1:p.Cys326Phe
ENST00000678614.1:n.236G>T
ENST00000678710.1:c.977G>T	ENSP00000504254.1:p.Cys326Phe
ENST00000678872.1:c.977G>T	ENSP00000503425.1:p.Cys326Phe
ENST00000678946.1:n.909G>T
ENST00000678953.1:c.*713G>T	ENSP00000504169.1:n.*713G>T
ENST00000679011.1:c.880G>T	ENSP00000503980.1:p.Val294Leu
ENST00000679024.1:c.977G>T	ENSP00000503506.1:p.Cys326Phe
ENST00000679160.1:c.902G>T	ENSP00000503972.1:p.Cys301Phe
ENST00000679225.1:n.917G>T
ENST00000679314.1:c.977G>T	ENSP00000503465.1:p.Cys326Phe
ENST00000679347.1:c.977G>T	ENSP00000503676.1:p.Cys326Phe
ENST00000310325.9:c.977G>T	ENSP00000310832.5:p.Cys326Phe
ENST00000524994.5:c.519G>T
ENST00000525733.5:c.244G>T
ENST00000527141.5:n.498G>T
ENST00000529199.1:n.316G>T
ENST00000530565.5:n.302G>T
NM_003793.3:c.977G>T	NP_003784.2:p.Cys326Phe
XM_011545328.1:c.797G>T	XP_011543630.1:p.Cys266Phe
XM_011545328.2:c.797G>T	XP_011543630.1:p.Cys266Phe
NM_003793.4:c.977G>T MANE Select	NP_003784.2:p.Cys326Phe