Canonical Allele Identifier: CA223827833

Gene: STIP1

Linked Data

• dbSNP Id: rs1013217549
• gnomAD v3: 11-64196389-C-CTT
• gnomAD v4: 11-64196389-C-CTT
• MyVariant Identifiers: chr11:g.63963861_63963862insTT (hg19) ; chr11:g.64196389_64196390insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196389_64196390insTT , CM000673.2:g.64196389_64196390insTT	GRCh38
NC_000011.9:g.63963861_63963862insTT , CM000673.1:g.63963861_63963862insTT	GRCh37
NC_000011.8:g.63720437_63720438insTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000305218.9:c.672+576_672+577insTT MANE Select	ENSP00000305958.5:n.672+576_672+577insTT
ENST00000305218.8:c.672+576_672+577insTT	ENSP00000305958.4:n.672+576_672+577insTT
ENST00000358794.9:c.813+576_813+577insTT	ENSP00000351646.5:n.813+576_813+577insTT
ENST00000536973.5:c.361+2059_361+2060insTT	ENSP00000441036.1:n.361+2059_361+2060insT...
ENST00000538945.5:c.600+576_600+577insTT	ENSP00000445957.1:n.600+576_600+577insTT
NM_001282652.1:c.813+576_813+577insTT	NP_001269581.1:n.813+576_813+577insTT
NM_001282653.1:c.600+576_600+577insTT	NP_001269582.1:n.600+576_600+577insTT
NM_006819.2:c.672+576_672+577insTT	NP_006810.1:n.672+576_672+577insTT
NM_001282653.2:c.600+576_600+577insTT	NP_001269582.1:n.600+576_600+577insTT
NM_006819.3:c.672+576_672+577insTT MANE Select	NP_006810.1:n.672+576_672+577insTT
NM_001282652.2:c.813+576_813+577insTT	NP_001269581.1:n.813+576_813+577insTT