Canonical Allele Identifier: CA938815254

Gene: STIP1

Linked Data

• gnomAD v3: 11-64196271-CT-C
• gnomAD v4: 11-64196271-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196272del , CM000673.2:g.64196272del	GRCh38
NC_000011.9:g.63963744del , CM000673.1:g.63963744del	GRCh37
NC_000011.8:g.63720320del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.672+459del MANE Select	ENSP00000305958.5:n.672+459del
ENST00000305218.8:c.672+459del	ENSP00000305958.4:n.672+459del
ENST00000358794.9:c.813+459del	ENSP00000351646.5:n.813+459del
ENST00000536973.5:c.361+1942del	ENSP00000441036.1:n.361+1942del
ENST00000538945.5:c.600+459del	ENSP00000445957.1:n.600+459del
NM_001282652.1:c.813+459del	NP_001269581.1:n.813+459del
NM_001282653.1:c.600+459del	NP_001269582.1:n.600+459del
NM_006819.2:c.672+459del	NP_006810.1:n.672+459del
NM_001282653.2:c.600+459del	NP_001269582.1:n.600+459del
NM_006819.3:c.672+459del MANE Select	NP_006810.1:n.672+459del
NM_001282652.2:c.813+459del	NP_001269581.1:n.813+459del