Canonical Allele Identifier: CA1978634589

Gene: STIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64196382C= , CM000673.2:g.64196382C=	GRCh38
NC_000011.9:g.63963854C= , CM000673.1:g.63963854C=	GRCh37
NC_000011.8:g.63720430C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000305218.9:c.672+569C= MANE Select	ENSP00000305958.5:n.672+569C=
ENST00000305218.8:c.672+569C=	ENSP00000305958.4:n.672+569C=
ENST00000358794.9:c.813+569C=	ENSP00000351646.5:n.813+569C=
ENST00000536973.5:c.361+2052C=	ENSP00000441036.1:n.361+2052C=
ENST00000538945.5:c.600+569C=	ENSP00000445957.1:n.600+569C=
NM_001282652.1:c.813+569C=	NP_001269581.1:n.813+569C=
NM_001282653.1:c.600+569C=	NP_001269582.1:n.600+569C=
NM_006819.2:c.672+569C=	NP_006810.1:n.672+569C=
NM_001282653.2:c.600+569C=	NP_001269582.1:n.600+569C=
NM_006819.3:c.672+569C= MANE Select	NP_006810.1:n.672+569C=
NM_001282652.2:c.813+569C=	NP_001269581.1:n.813+569C=