Canonical Allele Identifier: CA679246661

Gene: STIP1

Linked Data

• dbSNP Id: rs1245896835
• gnomAD v3: 11-64196412-AAAG-A
• gnomAD v4: 11-64196412-AAAG-A
• MyVariant Identifiers: chr11:g.63963885_63963887del (hg19) ; chr11:g.64196413_64196415del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196413_64196415del , CM000673.2:g.64196413_64196415del	GRCh38
NC_000011.9:g.63963885_63963887del , CM000673.1:g.63963885_63963887del	GRCh37
NC_000011.8:g.63720461_63720463del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+600_672+602del MANE Select	ENSP00000305958.5:n.672+600_672+602del
ENST00000305218.8:c.672+600_672+602del	ENSP00000305958.4:n.672+600_672+602del
ENST00000358794.9:c.813+600_813+602del	ENSP00000351646.5:n.813+600_813+602del
ENST00000536973.5:c.361+2083_361+2085del	ENSP00000441036.1:n.361+2083_361+2085del
ENST00000538945.5:c.600+600_600+602del	ENSP00000445957.1:n.600+600_600+602del
NM_001282652.1:c.813+600_813+602del	NP_001269581.1:n.813+600_813+602del
NM_001282653.1:c.600+600_600+602del	NP_001269582.1:n.600+600_600+602del
NM_006819.2:c.672+600_672+602del	NP_006810.1:n.672+600_672+602del
NM_001282653.2:c.600+600_600+602del	NP_001269582.1:n.600+600_600+602del
NM_006819.3:c.672+600_672+602del MANE Select	NP_006810.1:n.672+600_672+602del
NM_001282652.2:c.813+600_813+602del	NP_001269581.1:n.813+600_813+602del