Canonical Allele Identifier: CA1978635102

Gene: STIP1

Linked Data

• dbSNP Id: rs1591010610

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196499C>T , CM000673.2:g.64196499C>T	GRCh38
NC_000011.9:g.63963971C>T , CM000673.1:g.63963971C>T	GRCh37
NC_000011.8:g.63720547C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000305218.9:c.672+686C>T MANE Select	ENSP00000305958.5:n.672+686C>T
ENST00000305218.8:c.672+686C>T	ENSP00000305958.4:n.672+686C>T
ENST00000358794.9:c.813+686C>T	ENSP00000351646.5:n.813+686C>T
ENST00000536973.5:c.361+2169C>T	ENSP00000441036.1:n.361+2169C>T
ENST00000538945.5:c.600+686C>T	ENSP00000445957.1:n.600+686C>T
NM_001282652.1:c.813+686C>T	NP_001269581.1:n.813+686C>T
NM_001282653.1:c.600+686C>T	NP_001269582.1:n.600+686C>T
NM_006819.2:c.672+686C>T	NP_006810.1:n.672+686C>T
NM_001282653.2:c.600+686C>T	NP_001269582.1:n.600+686C>T
NM_006819.3:c.672+686C>T MANE Select	NP_006810.1:n.672+686C>T
NM_001282652.2:c.813+686C>T	NP_001269581.1:n.813+686C>T