Canonical Allele Identifier: CA223827836
Gene: STIP1 HGNC NCBI

Linked Data

dbSNP Id: rs867036814
gnomAD v2: 11-63963867-C-A
gnomAD v3: 11-64196395-C-A
gnomAD v4: 11-64196395-C-A
MyVariant Identifiers: chr11:g.63963867C>A (hg19) chr11:g.63963867_63963870delinsAAAA (hg19) chr11:g.64196395C>A (hg38) chr11:g.64196395_64196398delinsAAAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64196395C>A , CM000673.2:g.64196395C>A GRCh38
NC_000011.9:g.63963867C>A , CM000673.1:g.63963867C>A GRCh37
NC_000011.8:g.63720443C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305218.9:c.672+582C>A MANE Select ENSP00000305958.5:n.672+582C>A
ENST00000305218.8:c.672+582C>A ENSP00000305958.4:n.672+582C>A
ENST00000358794.9:c.813+582C>A ENSP00000351646.5:n.813+582C>A
ENST00000536973.5:c.361+2065C>A ENSP00000441036.1:n.361+2065C>A
ENST00000538945.5:c.600+582C>A ENSP00000445957.1:n.600+582C>A
NM_001282652.1:c.813+582C>A NP_001269581.1:n.813+582C>A
NM_001282653.1:c.600+582C>A NP_001269582.1:n.600+582C>A
NM_006819.2:c.672+582C>A NP_006810.1:n.672+582C>A
NM_001282653.2:c.600+582C>A NP_001269582.1:n.600+582C>A
NM_006819.3:c.672+582C>A MANE Select NP_006810.1:n.672+582C>A
NM_001282652.2:c.813+582C>A NP_001269581.1:n.813+582C>A
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