Canonical Allele Identifier: CA381460612

Gene: CTSF

Linked Data

• MyVariant Identifiers: chr11:g.66333305G>T (hg19) ; chr11:g.66565834G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.66565834G>T , CM000673.2:g.66565834G>T	GRCh38
NC_000011.9:g.66333305G>T , CM000673.1:g.66333305G>T	GRCh37
NC_000011.8:g.66089881G>T	NCBI36
NG_032973.1:g.7743C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310325.10:c.961C>A MANE Select	ENSP00000310832.5:p.Gln321Lys
ENST00000524994.6:c.958C>A	ENSP00000433082.2:p.Gln320Lys
ENST00000525733.6:c.*155C>A	ENSP00000434936.2:n.*155C>A
ENST00000526010.2:c.685C>A	ENSP00000435822.2:p.Gln229Lys
ENST00000527141.6:n.860C>A
ENST00000530565.6:n.584C>A
ENST00000533168.2:n.1049C>A
ENST00000676860.1:n.912C>A
ENST00000676924.1:c.961C>A	ENSP00000503579.1:p.Gln321Lys
ENST00000677005.1:c.961C>A	ENSP00000503238.1:p.Gln321Lys
ENST00000677186.1:n.1081C>A
ENST00000677298.1:n.1367C>A
ENST00000677365.1:n.1020C>A
ENST00000677526.1:c.868-83C>A	ENSP00000504693.1:n.868-83C>A
ENST00000677587.1:c.1003C>A	ENSP00000503791.1:p.Gln335Lys
ENST00000677779.1:n.806C>A
ENST00000677896.1:c.952C>A	ENSP00000504605.1:p.Gln318Lys
ENST00000677920.1:c.*213C>A	ENSP00000503614.1:n.*213C>A
ENST00000678154.1:c.*623C>A	ENSP00000502935.1:n.*623C>A
ENST00000678294.1:n.1077C>A
ENST00000678305.1:c.889C>A	ENSP00000504383.1:p.Gln297Lys
ENST00000678383.1:n.970C>A
ENST00000678413.1:c.*155C>A	ENSP00000503232.1:n.*155C>A
ENST00000678471.1:c.961C>A	ENSP00000502949.1:p.Gln321Lys
ENST00000678614.1:n.141C>A
ENST00000678710.1:c.961C>A	ENSP00000504254.1:p.Gln321Lys
ENST00000678872.1:c.961C>A	ENSP00000503425.1:p.Gln321Lys
ENST00000678946.1:n.893C>A
ENST00000678953.1:c.*697C>A	ENSP00000504169.1:n.*697C>A
ENST00000679011.1:c.868-83C>A	ENSP00000503980.1:n.868-83C>A
ENST00000679024.1:c.961C>A	ENSP00000503506.1:p.Gln321Lys
ENST00000679160.1:c.886C>A	ENSP00000503972.1:p.Gln296Lys
ENST00000679225.1:n.901C>A
ENST00000679314.1:c.961C>A	ENSP00000503465.1:p.Gln321Lys
ENST00000679347.1:c.961C>A	ENSP00000503676.1:p.Gln321Lys
ENST00000310325.9:c.961C>A	ENSP00000310832.5:p.Gln321Lys
ENST00000524994.5:c.503C>A
ENST00000525733.5:c.230C>A
ENST00000527141.5:n.482C>A
ENST00000529199.1:n.221C>A
ENST00000530565.5:n.207C>A
NM_003793.3:c.961C>A	NP_003784.2:p.Gln321Lys
XM_011545328.1:c.781C>A	XP_011543630.1:p.Gln261Lys
XM_011545328.2:c.781C>A	XP_011543630.1:p.Gln261Lys
NM_003793.4:c.961C>A MANE Select	NP_003784.2:p.Gln321Lys