Canonical Allele Identifier: CA2792412017

Gene: STIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196396_64196397insG , CM000673.2:g.64196396_64196397insG	GRCh38
NC_000011.9:g.63963868_63963869insG , CM000673.1:g.63963868_63963869insG	GRCh37
NC_000011.8:g.63720444_63720445insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+583_672+584insG MANE Select	ENSP00000305958.5:n.672+583_672+584insG
ENST00000305218.8:c.672+583_672+584insG	ENSP00000305958.4:n.672+583_672+584insG
ENST00000358794.9:c.813+583_813+584insG	ENSP00000351646.5:n.813+583_813+584insG
ENST00000536973.5:c.361+2066_361+2067insG	ENSP00000441036.1:n.361+2066_361+2067insG
ENST00000538945.5:c.600+583_600+584insG	ENSP00000445957.1:n.600+583_600+584insG
NM_001282652.1:c.813+583_813+584insG	NP_001269581.1:n.813+583_813+584insG
NM_001282653.1:c.600+583_600+584insG	NP_001269582.1:n.600+583_600+584insG
NM_006819.2:c.672+583_672+584insG	NP_006810.1:n.672+583_672+584insG
NM_001282653.2:c.600+583_600+584insG	NP_001269582.1:n.600+583_600+584insG
NM_006819.3:c.672+583_672+584insG MANE Select	NP_006810.1:n.672+583_672+584insG
NM_001282652.2:c.813+583_813+584insG	NP_001269581.1:n.813+583_813+584insG