Canonical Allele Identifier: CA1978634558
Gene: STIP1 HGNC NCBI

Linked Data

dbSNP Id: rs1946150082
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64196360del , CM000673.2:g.64196360del GRCh38
NC_000011.9:g.63963832del , CM000673.1:g.63963832del GRCh37
NC_000011.8:g.63720408del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000305218.9:c.672+547del MANE Select ENSP00000305958.5:n.672+547del
ENST00000305218.8:c.672+547del ENSP00000305958.4:n.672+547del
ENST00000358794.9:c.813+547del ENSP00000351646.5:n.813+547del
ENST00000536973.5:c.361+2030del ENSP00000441036.1:n.361+2030del
ENST00000538945.5:c.600+547del ENSP00000445957.1:n.600+547del
NM_001282652.1:c.813+547del NP_001269581.1:n.813+547del
NM_001282653.1:c.600+547del NP_001269582.1:n.600+547del
NM_006819.2:c.672+547del NP_006810.1:n.672+547del
NM_001282653.2:c.600+547del NP_001269582.1:n.600+547del
NM_006819.3:c.672+547del MANE Select NP_006810.1:n.672+547del
NM_001282652.2:c.813+547del NP_001269581.1:n.813+547del
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