Canonical Allele Identifier: CA2525229806
Gene: STIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64196383del , CM000673.2:g.64196383del GRCh38
NC_000011.9:g.63963855del , CM000673.1:g.63963855del GRCh37
NC_000011.8:g.63720431del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305218.9:c.672+570del MANE Select ENSP00000305958.5:n.672+570del
ENST00000305218.8:c.672+570del ENSP00000305958.4:n.672+570del
ENST00000358794.9:c.813+570del ENSP00000351646.5:n.813+570del
ENST00000536973.5:c.361+2053del ENSP00000441036.1:n.361+2053del
ENST00000538945.5:c.600+570del ENSP00000445957.1:n.600+570del
NM_001282652.1:c.813+570del NP_001269581.1:n.813+570del
NM_001282653.1:c.600+570del NP_001269582.1:n.600+570del
NM_006819.2:c.672+570del NP_006810.1:n.672+570del
NM_001282653.2:c.600+570del NP_001269582.1:n.600+570del
NM_006819.3:c.672+570del MANE Select NP_006810.1:n.672+570del
NM_001282652.2:c.813+570del NP_001269581.1:n.813+570del