Canonical Allele Identifier: CA1978634339

Gene: STIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196210_64196223delinsACATGGTGAAACCT , CM000673.2:g.64196210_64196223delinsACATGGTGAAACCT	GRCh38
NC_000011.9:g.63963682_63963695delinsACATGGTGAAACCT , CM000673.1:g.63963682_63963695delinsACATGGTGAAACCT	GRCh37
NC_000011.8:g.63720258_63720271delinsACATGGTGAAACCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+397_672+410delinsACATGGTGAAACCT MANE Select	ENSP00000305958.5:n.672+397_672+410delinsACATGGTGAAACCT
ENST00000305218.8:c.672+397_672+410delinsACATGGTGAAACCT	ENSP00000305958.4:n.672+397_672+410delinsACATGGTGAAACCT
ENST00000358794.9:c.813+397_813+410delinsACATGGTGAAACCT	ENSP00000351646.5:n.813+397_813+410delinsACATGGTGAAACCT
ENST00000536973.5:c.361+1880_361+1893delinsACATGGTGAAACCT	ENSP00000441036.1:n.361+1880_361+1893delinsACATGGTGAAACCT
ENST00000538945.5:c.600+397_600+410delinsACATGGTGAAACCT	ENSP00000445957.1:n.600+397_600+410delinsACATGGTGAAACCT
NM_001282652.1:c.813+397_813+410delinsACATGGTGAAACCT	NP_001269581.1:n.813+397_813+410delinsACATGGTGAAACCT
NM_001282653.1:c.600+397_600+410delinsACATGGTGAAACCT	NP_001269582.1:n.600+397_600+410delinsACATGGTGAAACCT
NM_006819.2:c.672+397_672+410delinsACATGGTGAAACCT	NP_006810.1:n.672+397_672+410delinsACATGGTGAAACCT
NM_001282653.2:c.600+397_600+410delinsACATGGTGAAACCT	NP_001269582.1:n.600+397_600+410delinsACATGGTGAAACCT
NM_006819.3:c.672+397_672+410delinsACATGGTGAAACCT MANE Select	NP_006810.1:n.672+397_672+410delinsACATGGTGAAACCT
NM_001282652.2:c.813+397_813+410delinsACATGGTGAAACCT	NP_001269581.1:n.813+397_813+410delinsACATGGTGAAACCT