Canonical Allele Identifier: CA1978635029

Gene: STIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196449_64196451delinsCAA , CM000673.2:g.64196449_64196451delinsCAA	GRCh38
NC_000011.9:g.63963921_63963923delinsCAA , CM000673.1:g.63963921_63963923delinsCAA	GRCh37
NC_000011.8:g.63720497_63720499delinsCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+636_672+638delinsCAA MANE Select	ENSP00000305958.5:n.672+636_672+638delinsCAA
ENST00000305218.8:c.672+636_672+638delinsCAA	ENSP00000305958.4:n.672+636_672+638delinsCAA
ENST00000358794.9:c.813+636_813+638delinsCAA	ENSP00000351646.5:n.813+636_813+638delinsCAA
ENST00000536973.5:c.361+2119_361+2121delinsCAA	ENSP00000441036.1:n.361+2119_361+2121delinsCAA
ENST00000538945.5:c.600+636_600+638delinsCAA	ENSP00000445957.1:n.600+636_600+638delinsCAA
NM_001282652.1:c.813+636_813+638delinsCAA	NP_001269581.1:n.813+636_813+638delinsCAA
NM_001282653.1:c.600+636_600+638delinsCAA	NP_001269582.1:n.600+636_600+638delinsCAA
NM_006819.2:c.672+636_672+638delinsCAA	NP_006810.1:n.672+636_672+638delinsCAA
NM_001282653.2:c.600+636_600+638delinsCAA	NP_001269582.1:n.600+636_600+638delinsCAA
NM_006819.3:c.672+636_672+638delinsCAA MANE Select	NP_006810.1:n.672+636_672+638delinsCAA
NM_001282652.2:c.813+636_813+638delinsCAA	NP_001269581.1:n.813+636_813+638delinsCAA