Canonical Allele Identifier: CA679242433

Gene: STIP1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64191787A>T , CM000673.2:g.64191787A>T	GRCh38
NC_000011.9:g.63959259A>T , CM000673.1:g.63959259A>T	GRCh37
NC_000011.8:g.63715835A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305218.9:c.10-1291A>T MANE Select	ENSP00000305958.5:n.10-1291A>T
ENST00000305218.8:c.10-1291A>T	ENSP00000305958.4:n.10-1291A>T
ENST00000358794.9:c.151-1291A>T	ENSP00000351646.5:n.151-1291A>T
ENST00000536973.5:c.10-1291A>T	ENSP00000441036.1:n.10-1291A>T
ENST00000538945.5:c.10-1291A>T	ENSP00000445957.1:n.10-1291A>T
ENST00000540501.1:n.220-1291A>T
ENST00000540736.1:n.38-1291A>T
ENST00000543847.1:c.10-1291A>T	ENSP00000442704.1:n.10-1291A>T
NM_001282652.1:c.151-1291A>T	NP_001269581.1:n.151-1291A>T
NM_001282653.1:c.10-1291A>T	NP_001269582.1:n.10-1291A>T
NM_006819.2:c.10-1291A>T	NP_006810.1:n.10-1291A>T
NM_001282653.2:c.10-1291A>T	NP_001269582.1:n.10-1291A>T
NM_006819.3:c.10-1291A>T MANE Select	NP_006810.1:n.10-1291A>T
NM_001282652.2:c.151-1291A>T	NP_001269581.1:n.151-1291A>T