Canonical Allele Identifier: CA381460350

Gene: CTSF

Linked Data

• MyVariant Identifiers: chr11:g.66333213T>G (hg19) ; chr11:g.66565742T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66565742T>G , CM000673.2:g.66565742T>G	GRCh38
NC_000011.9:g.66333213T>G , CM000673.1:g.66333213T>G	GRCh37
NC_000011.8:g.66089789T>G	NCBI36
NG_032973.1:g.7835A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310325.10:c.974A>C MANE Select	ENSP00000310832.5:p.Asp325Ala
ENST00000524994.6:c.971A>C	ENSP00000433082.2:p.Asp324Ala
ENST00000525733.6:c.*168A>C	ENSP00000434936.2:n.*168A>C
ENST00000526010.2:c.698A>C	ENSP00000435822.2:p.Asp233Ala
ENST00000527141.6:n.873A>C
ENST00000530565.6:n.676A>C
ENST00000533168.2:n.1062A>C
ENST00000676860.1:n.925A>C
ENST00000676924.1:c.972A>C	ENSP00000503579.1:p.Gly324=
ENST00000677005.1:c.974A>C	ENSP00000503238.1:p.Asp325Ala
ENST00000677186.1:n.1094A>C
ENST00000677298.1:n.1380A>C
ENST00000677365.1:n.1112A>C
ENST00000677526.1:c.877A>C	ENSP00000504693.1:p.Thr293Pro
ENST00000677587.1:c.1016A>C	ENSP00000503791.1:p.Asp339Ala
ENST00000677779.1:n.819A>C
ENST00000677896.1:c.965A>C	ENSP00000504605.1:p.Asp322Ala
ENST00000677920.1:c.*226A>C	ENSP00000503614.1:n.*226A>C
ENST00000678154.1:c.*636A>C	ENSP00000502935.1:n.*636A>C
ENST00000678294.1:n.1090A>C
ENST00000678305.1:c.902A>C	ENSP00000504383.1:p.Asp301Ala
ENST00000678383.1:n.1062A>C
ENST00000678413.1:c.*168A>C	ENSP00000503232.1:n.*168A>C
ENST00000678471.1:c.974A>C	ENSP00000502949.1:p.Asp325Ala
ENST00000678614.1:n.233A>C
ENST00000678710.1:c.974A>C	ENSP00000504254.1:p.Asp325Ala
ENST00000678872.1:c.974A>C	ENSP00000503425.1:p.Asp325Ala
ENST00000678946.1:n.906A>C
ENST00000678953.1:c.*710A>C	ENSP00000504169.1:n.*710A>C
ENST00000679011.1:c.877A>C	ENSP00000503980.1:p.Thr293Pro
ENST00000679024.1:c.974A>C	ENSP00000503506.1:p.Asp325Ala
ENST00000679160.1:c.899A>C	ENSP00000503972.1:p.Asp300Ala
ENST00000679225.1:n.914A>C
ENST00000679314.1:c.974A>C	ENSP00000503465.1:p.Asp325Ala
ENST00000679347.1:c.974A>C	ENSP00000503676.1:p.Asp325Ala
ENST00000310325.9:c.974A>C	ENSP00000310832.5:p.Asp325Ala
ENST00000524994.5:c.516A>C
ENST00000525733.5:c.241A>C
ENST00000527141.5:n.495A>C
ENST00000529199.1:n.313A>C
ENST00000530565.5:n.299A>C
NM_003793.3:c.974A>C	NP_003784.2:p.Asp325Ala
XM_011545328.1:c.794A>C	XP_011543630.1:p.Asp265Ala
XM_011545328.2:c.794A>C	XP_011543630.1:p.Asp265Ala
NM_003793.4:c.974A>C MANE Select	NP_003784.2:p.Asp325Ala