Canonical Allele Identifier: CA2792412012

Gene: STIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196266_64196267insCGT , CM000673.2:g.64196266_64196267insCGT	GRCh38
NC_000011.9:g.63963738_63963739insCGT , CM000673.1:g.63963738_63963739insCGT	GRCh37
NC_000011.8:g.63720314_63720315insCGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+453_672+454insCGT MANE Select	ENSP00000305958.5:n.672+453_672+454insCGT
ENST00000305218.8:c.672+453_672+454insCGT	ENSP00000305958.4:n.672+453_672+454insCGT
ENST00000358794.9:c.813+453_813+454insCGT	ENSP00000351646.5:n.813+453_813+454insCGT
ENST00000536973.5:c.361+1936_361+1937insCGT	ENSP00000441036.1:n.361+1936_361+1937insCGT
ENST00000538945.5:c.600+453_600+454insCGT	ENSP00000445957.1:n.600+453_600+454insCGT
NM_001282652.1:c.813+453_813+454insCGT	NP_001269581.1:n.813+453_813+454insCGT
NM_001282653.1:c.600+453_600+454insCGT	NP_001269582.1:n.600+453_600+454insCGT
NM_006819.2:c.672+453_672+454insCGT	NP_006810.1:n.672+453_672+454insCGT
NM_001282653.2:c.600+453_600+454insCGT	NP_001269582.1:n.600+453_600+454insCGT
NM_006819.3:c.672+453_672+454insCGT MANE Select	NP_006810.1:n.672+453_672+454insCGT
NM_001282652.2:c.813+453_813+454insCGT	NP_001269581.1:n.813+453_813+454insCGT