Canonical Allele Identifier: CA1978634848
Gene: STIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64196394_64196395delinsTC , CM000673.2:g.64196394_64196395delinsTC GRCh38
NC_000011.9:g.63963866_63963867delinsTC , CM000673.1:g.63963866_63963867delinsTC GRCh37
NC_000011.8:g.63720442_63720443delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305218.9:c.672+581_672+582delinsTC MANE Select ENSP00000305958.5:n.672+581_672+582delins...
ENST00000305218.8:c.672+581_672+582delinsTC ENSP00000305958.4:n.672+581_672+582delins...
ENST00000358794.9:c.813+581_813+582delinsTC ENSP00000351646.5:n.813+581_813+582delins...
ENST00000536973.5:c.361+2064_361+2065delinsTC ENSP00000441036.1:n.361+2064_361+2065deli...
ENST00000538945.5:c.600+581_600+582delinsTC ENSP00000445957.1:n.600+581_600+582delins...
NM_001282652.1:c.813+581_813+582delinsTC NP_001269581.1:n.813+581_813+582delinsTC
NM_001282653.1:c.600+581_600+582delinsTC NP_001269582.1:n.600+581_600+582delinsTC
NM_006819.2:c.672+581_672+582delinsTC NP_006810.1:n.672+581_672+582delinsTC
NM_001282653.2:c.600+581_600+582delinsTC NP_001269582.1:n.600+581_600+582delinsTC
NM_006819.3:c.672+581_672+582delinsTC MANE Select NP_006810.1:n.672+581_672+582delinsTC
NM_001282652.2:c.813+581_813+582delinsTC NP_001269581.1:n.813+581_813+582delinsTC