Canonical Allele Identifier: CA938815376

Gene: STIP1

Linked Data

• dbSNP Id: rs1946150461
• gnomAD v3: 11-64196393-CT-C
• gnomAD v4: 11-64196393-CT-C

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000305218.9:c.672+581del MANE Select	ENSP00000305958.5:n.672+581del
ENST00000305218.8:c.672+581del	ENSP00000305958.4:n.672+581del
ENST00000358794.9:c.813+581del	ENSP00000351646.5:n.813+581del
ENST00000536973.5:c.361+2064del	ENSP00000441036.1:n.361+2064del
ENST00000538945.5:c.600+581del	ENSP00000445957.1:n.600+581del
NM_001282652.1:c.813+581del	NP_001269581.1:n.813+581del
NM_001282653.1:c.600+581del	NP_001269582.1:n.600+581del
NM_006819.2:c.672+581del	NP_006810.1:n.672+581del
NM_001282653.2:c.600+581del	NP_001269582.1:n.600+581del
NM_006819.3:c.672+581del MANE Select	NP_006810.1:n.672+581del
NM_001282652.2:c.813+581del	NP_001269581.1:n.813+581del