Canonical Allele Identifier: CA938815374

Gene: STIP1

Linked Data

• gnomAD v3: 11-64196393-C-CT
• gnomAD v4: 11-64196393-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196394dup , CM000673.2:g.64196394dup	GRCh38
NC_000011.9:g.63963866dup , CM000673.1:g.63963866dup	GRCh37
NC_000011.8:g.63720442dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000305218.9:c.672+581dup MANE Select	ENSP00000305958.5:n.672+581dup
ENST00000305218.8:c.672+581dup	ENSP00000305958.4:n.672+581dup
ENST00000358794.9:c.813+581dup	ENSP00000351646.5:n.813+581dup
ENST00000536973.5:c.361+2064dup	ENSP00000441036.1:n.361+2064dup
ENST00000538945.5:c.600+581dup	ENSP00000445957.1:n.600+581dup
NM_001282652.1:c.813+581dup	NP_001269581.1:n.813+581dup
NM_001282653.1:c.600+581dup	NP_001269582.1:n.600+581dup
NM_006819.2:c.672+581dup	NP_006810.1:n.672+581dup
NM_001282653.2:c.600+581dup	NP_001269582.1:n.600+581dup
NM_006819.3:c.672+581dup MANE Select	NP_006810.1:n.672+581dup
NM_001282652.2:c.813+581dup	NP_001269581.1:n.813+581dup