Canonical Allele Identifier: CA938815226

Gene: STIP1

Linked Data

• gnomAD v3: 11-64196258-T-TA
• gnomAD v4: 11-64196258-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196258_64196259insA , CM000673.2:g.64196258_64196259insA	GRCh38
NC_000011.9:g.63963730_63963731insA , CM000673.1:g.63963730_63963731insA	GRCh37
NC_000011.8:g.63720306_63720307insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+445_672+446insA MANE Select	ENSP00000305958.5:n.672+445_672+446insA
ENST00000305218.8:c.672+445_672+446insA	ENSP00000305958.4:n.672+445_672+446insA
ENST00000358794.9:c.813+445_813+446insA	ENSP00000351646.5:n.813+445_813+446insA
ENST00000536973.5:c.361+1928_361+1929insA	ENSP00000441036.1:n.361+1928_361+1929insA
ENST00000538945.5:c.600+445_600+446insA	ENSP00000445957.1:n.600+445_600+446insA
NM_001282652.1:c.813+445_813+446insA	NP_001269581.1:n.813+445_813+446insA
NM_001282653.1:c.600+445_600+446insA	NP_001269582.1:n.600+445_600+446insA
NM_006819.2:c.672+445_672+446insA	NP_006810.1:n.672+445_672+446insA
NM_001282653.2:c.600+445_600+446insA	NP_001269582.1:n.600+445_600+446insA
NM_006819.3:c.672+445_672+446insA MANE Select	NP_006810.1:n.672+445_672+446insA
NM_001282652.2:c.813+445_813+446insA	NP_001269581.1:n.813+445_813+446insA