Canonical Allele Identifier: CA1978634869

Gene: STIP1

Linked Data

• dbSNP Id: rs1946150574

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196395_64196396del , CM000673.2:g.64196395_64196396del	GRCh38
NC_000011.9:g.63963867_63963868del , CM000673.1:g.63963867_63963868del	GRCh37
NC_000011.8:g.63720443_63720444del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000305218.9:c.672+582_672+583del MANE Select	ENSP00000305958.5:n.672+582_672+583del
ENST00000305218.8:c.672+582_672+583del	ENSP00000305958.4:n.672+582_672+583del
ENST00000358794.9:c.813+582_813+583del	ENSP00000351646.5:n.813+582_813+583del
ENST00000536973.5:c.361+2065_361+2066del	ENSP00000441036.1:n.361+2065_361+2066del
ENST00000538945.5:c.600+582_600+583del	ENSP00000445957.1:n.600+582_600+583del
NM_001282652.1:c.813+582_813+583del	NP_001269581.1:n.813+582_813+583del
NM_001282653.1:c.600+582_600+583del	NP_001269582.1:n.600+582_600+583del
NM_006819.2:c.672+582_672+583del	NP_006810.1:n.672+582_672+583del
NM_001282653.2:c.600+582_600+583del	NP_001269582.1:n.600+582_600+583del
NM_006819.3:c.672+582_672+583del MANE Select	NP_006810.1:n.672+582_672+583del
NM_001282652.2:c.813+582_813+583del	NP_001269581.1:n.813+582_813+583del