Canonical Allele Identifier: CA654213224

Gene: STIP1

Linked Data

• COSMIC: COSN22904622

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196243_64196246del , CM000673.2:g.64196243_64196246del	GRCh38
NC_000011.9:g.63963715_63963718del , CM000673.1:g.63963715_63963718del	GRCh37
NC_000011.8:g.63720291_63720294del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+430_672+433del MANE Select	ENSP00000305958.5:n.672+430_672+433del
ENST00000305218.8:c.672+430_672+433del	ENSP00000305958.4:n.672+430_672+433del
ENST00000358794.9:c.813+430_813+433del	ENSP00000351646.5:n.813+430_813+433del
ENST00000536973.5:c.361+1913_361+1916del	ENSP00000441036.1:n.361+1913_361+1916del
ENST00000538945.5:c.600+430_600+433del	ENSP00000445957.1:n.600+430_600+433del
NM_001282652.1:c.813+430_813+433del	NP_001269581.1:n.813+430_813+433del
NM_001282653.1:c.600+430_600+433del	NP_001269582.1:n.600+430_600+433del
NM_006819.2:c.672+430_672+433del	NP_006810.1:n.672+430_672+433del
NM_001282653.2:c.600+430_600+433del	NP_001269582.1:n.600+430_600+433del
NM_006819.3:c.672+430_672+433del MANE Select	NP_006810.1:n.672+430_672+433del
NM_001282652.2:c.813+430_813+433del	NP_001269581.1:n.813+430_813+433del