Canonical Allele Identifier: CA938815246

Gene: STIP1

Linked Data

• gnomAD v3: 11-64196261-T-TCTC
• gnomAD v4: 11-64196261-T-TCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196261_64196262insCTC , CM000673.2:g.64196261_64196262insCTC	GRCh38
NC_000011.9:g.63963733_63963734insCTC , CM000673.1:g.63963733_63963734insCTC	GRCh37
NC_000011.8:g.63720309_63720310insCTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+448_672+449insCTC MANE Select	ENSP00000305958.5:n.672+448_672+449insCTC
ENST00000305218.8:c.672+448_672+449insCTC	ENSP00000305958.4:n.672+448_672+449insCTC
ENST00000358794.9:c.813+448_813+449insCTC	ENSP00000351646.5:n.813+448_813+449insCTC
ENST00000536973.5:c.361+1931_361+1932insCTC	ENSP00000441036.1:n.361+1931_361+1932insCTC
ENST00000538945.5:c.600+448_600+449insCTC	ENSP00000445957.1:n.600+448_600+449insCTC
NM_001282652.1:c.813+448_813+449insCTC	NP_001269581.1:n.813+448_813+449insCTC
NM_001282653.1:c.600+448_600+449insCTC	NP_001269582.1:n.600+448_600+449insCTC
NM_006819.2:c.672+448_672+449insCTC	NP_006810.1:n.672+448_672+449insCTC
NM_001282653.2:c.600+448_600+449insCTC	NP_001269582.1:n.600+448_600+449insCTC
NM_006819.3:c.672+448_672+449insCTC MANE Select	NP_006810.1:n.672+448_672+449insCTC
NM_001282652.2:c.813+448_813+449insCTC	NP_001269581.1:n.813+448_813+449insCTC