Canonical Allele Identifier: CA1978635067

Gene: STIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196476_64196477delinsTC , CM000673.2:g.64196476_64196477delinsTC	GRCh38
NC_000011.9:g.63963948_63963949delinsTC , CM000673.1:g.63963948_63963949delinsTC	GRCh37
NC_000011.8:g.63720524_63720525delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+663_672+664delinsTC MANE Select	ENSP00000305958.5:n.672+663_672+664delinsTC
ENST00000305218.8:c.672+663_672+664delinsTC	ENSP00000305958.4:n.672+663_672+664delinsTC
ENST00000358794.9:c.813+663_813+664delinsTC	ENSP00000351646.5:n.813+663_813+664delinsTC
ENST00000536973.5:c.361+2146_361+2147delinsTC	ENSP00000441036.1:n.361+2146_361+2147delinsTC
ENST00000538945.5:c.600+663_600+664delinsTC	ENSP00000445957.1:n.600+663_600+664delinsTC
NM_001282652.1:c.813+663_813+664delinsTC	NP_001269581.1:n.813+663_813+664delinsTC
NM_001282653.1:c.600+663_600+664delinsTC	NP_001269582.1:n.600+663_600+664delinsTC
NM_006819.2:c.672+663_672+664delinsTC	NP_006810.1:n.672+663_672+664delinsTC
NM_001282653.2:c.600+663_600+664delinsTC	NP_001269582.1:n.600+663_600+664delinsTC
NM_006819.3:c.672+663_672+664delinsTC MANE Select	NP_006810.1:n.672+663_672+664delinsTC
NM_001282652.2:c.813+663_813+664delinsTC	NP_001269581.1:n.813+663_813+664delinsTC