Canonical Allele Identifier: CA599627814

Gene: STIP1

Linked Data

• dbSNP Id: rs57497154
• gnomAD v2: 11-63963867-CAAA-C
• gnomAD v3: 11-64196395-CAAA-C
• gnomAD v4: 11-64196395-CAAA-C
• MyVariant Identifiers: chr11:g.63963868_63963870del (hg19) ; chr11:g.64196396_64196398del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196412_64196414del , CM000673.2:g.64196412_64196414del	GRCh38
NC_000011.9:g.63963884_63963886del , CM000673.1:g.63963884_63963886del	GRCh37
NC_000011.8:g.63720460_63720462del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+599_672+601del MANE Select	ENSP00000305958.5:n.672+599_672+601del
ENST00000305218.8:c.672+599_672+601del	ENSP00000305958.4:n.672+599_672+601del
ENST00000358794.9:c.813+599_813+601del	ENSP00000351646.5:n.813+599_813+601del
ENST00000536973.5:c.361+2082_361+2084del	ENSP00000441036.1:n.361+2082_361+2084del
ENST00000538945.5:c.600+599_600+601del	ENSP00000445957.1:n.600+599_600+601del
NM_001282652.1:c.813+599_813+601del	NP_001269581.1:n.813+599_813+601del
NM_001282653.1:c.600+599_600+601del	NP_001269582.1:n.600+599_600+601del
NM_006819.2:c.672+599_672+601del	NP_006810.1:n.672+599_672+601del
NM_001282653.2:c.600+599_600+601del	NP_001269582.1:n.600+599_600+601del
NM_006819.3:c.672+599_672+601del MANE Select	NP_006810.1:n.672+599_672+601del
NM_001282652.2:c.813+599_813+601del	NP_001269581.1:n.813+599_813+601del