Canonical Allele Identifier: CA381460676

Gene: CTSF

Linked Data

• MyVariant Identifiers: chr11:g.66333310G>T (hg19) ; chr11:g.66565839G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66565839G>T , CM000673.2:g.66565839G>T	GRCh38
NC_000011.9:g.66333310G>T , CM000673.1:g.66333310G>T	GRCh37
NC_000011.8:g.66089886G>T	NCBI36
NG_032973.1:g.7738C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310325.10:c.956C>A MANE Select	ENSP00000310832.5:p.Ser319Tyr
ENST00000524994.6:c.953C>A	ENSP00000433082.2:p.Ser318Tyr
ENST00000525733.6:c.*150C>A	ENSP00000434936.2:n.*150C>A
ENST00000526010.2:c.680C>A	ENSP00000435822.2:p.Ser227Tyr
ENST00000527141.6:n.855C>A
ENST00000530565.6:n.579C>A
ENST00000533168.2:n.1044C>A
ENST00000676860.1:n.907C>A
ENST00000676924.1:c.956C>A	ENSP00000503579.1:p.Ser319Tyr
ENST00000677005.1:c.956C>A	ENSP00000503238.1:p.Ser319Tyr
ENST00000677186.1:n.1076C>A
ENST00000677298.1:n.1362C>A
ENST00000677365.1:n.1015C>A
ENST00000677526.1:c.868-88C>A	ENSP00000504693.1:n.868-88C>A
ENST00000677587.1:c.998C>A	ENSP00000503791.1:p.Ser333Tyr
ENST00000677779.1:n.801C>A
ENST00000677896.1:c.947C>A	ENSP00000504605.1:p.Ser316Tyr
ENST00000677920.1:c.*208C>A	ENSP00000503614.1:n.*208C>A
ENST00000678154.1:c.*618C>A	ENSP00000502935.1:n.*618C>A
ENST00000678294.1:n.1072C>A
ENST00000678305.1:c.884C>A	ENSP00000504383.1:p.Ser295Tyr
ENST00000678383.1:n.965C>A
ENST00000678413.1:c.*150C>A	ENSP00000503232.1:n.*150C>A
ENST00000678471.1:c.956C>A	ENSP00000502949.1:p.Ser319Tyr
ENST00000678614.1:n.136C>A
ENST00000678710.1:c.956C>A	ENSP00000504254.1:p.Ser319Tyr
ENST00000678872.1:c.956C>A	ENSP00000503425.1:p.Ser319Tyr
ENST00000678946.1:n.888C>A
ENST00000678953.1:c.*692C>A	ENSP00000504169.1:n.*692C>A
ENST00000679011.1:c.868-88C>A	ENSP00000503980.1:n.868-88C>A
ENST00000679024.1:c.956C>A	ENSP00000503506.1:p.Ser319Tyr
ENST00000679160.1:c.881C>A	ENSP00000503972.1:p.Ser294Tyr
ENST00000679225.1:n.896C>A
ENST00000679314.1:c.956C>A	ENSP00000503465.1:p.Ser319Tyr
ENST00000679347.1:c.956C>A	ENSP00000503676.1:p.Ser319Tyr
ENST00000310325.9:c.956C>A	ENSP00000310832.5:p.Ser319Tyr
ENST00000524994.5:c.498C>A
ENST00000525733.5:c.225C>A
ENST00000527141.5:n.477C>A
ENST00000529199.1:n.216C>A
ENST00000530565.5:n.202C>A
NM_003793.3:c.956C>A	NP_003784.2:p.Ser319Tyr
XM_011545328.1:c.776C>A	XP_011543630.1:p.Ser259Tyr
XM_011545328.2:c.776C>A	XP_011543630.1:p.Ser259Tyr
NM_003793.4:c.956C>A MANE Select	NP_003784.2:p.Ser319Tyr