Canonical Allele Identifier: CA599627813

Gene: STIP1

Linked Data

• dbSNP Id: rs1489100183
• gnomAD v2: 11-63963866-T-TA
• gnomAD v3: 11-64196394-T-TA
• gnomAD v4: 11-64196394-T-TA
• MyVariant Identifiers: chr11:g.63963866_63963867insA (hg19) ; chr11:g.64196394_64196395insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196394_64196395insA , CM000673.2:g.64196394_64196395insA	GRCh38
NC_000011.9:g.63963866_63963867insA , CM000673.1:g.63963866_63963867insA	GRCh37
NC_000011.8:g.63720442_63720443insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+581_672+582insA MANE Select	ENSP00000305958.5:n.672+581_672+582insA
ENST00000305218.8:c.672+581_672+582insA	ENSP00000305958.4:n.672+581_672+582insA
ENST00000358794.9:c.813+581_813+582insA	ENSP00000351646.5:n.813+581_813+582insA
ENST00000536973.5:c.361+2064_361+2065insA	ENSP00000441036.1:n.361+2064_361+2065insA
ENST00000538945.5:c.600+581_600+582insA	ENSP00000445957.1:n.600+581_600+582insA
NM_001282652.1:c.813+581_813+582insA	NP_001269581.1:n.813+581_813+582insA
NM_001282653.1:c.600+581_600+582insA	NP_001269582.1:n.600+581_600+582insA
NM_006819.2:c.672+581_672+582insA	NP_006810.1:n.672+581_672+582insA
NM_001282653.2:c.600+581_600+582insA	NP_001269582.1:n.600+581_600+582insA
NM_006819.3:c.672+581_672+582insA MANE Select	NP_006810.1:n.672+581_672+582insA
NM_001282652.2:c.813+581_813+582insA	NP_001269581.1:n.813+581_813+582insA