Canonical Allele Identifier: CA13532542
Gene: STIP1 HGNC NCBI

Linked Data

dbSNP Id: rs2236647

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64197133C>T , CM000673.2:g.64197133C>T GRCh38
NC_000011.9:g.63964605C>T , CM000673.1:g.63964605C>T GRCh37
NC_000011.8:g.63721181C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305218.9:c.673-138C>T MANE Select ENSP00000305958.5:n.673-138C>T
ENST00000305218.8:c.673-138C>T ENSP00000305958.4:n.673-138C>T
ENST00000358794.9:c.814-138C>T ENSP00000351646.5:n.814-138C>T
ENST00000536973.5:c.361+2803C>T ENSP00000441036.1:n.361+2803C>T
ENST00000537479.5:n.138C>T
ENST00000538945.5:c.601-138C>T ENSP00000445957.1:n.601-138C>T
ENST00000544739.5:n.211+87C>T
NM_001282652.1:c.814-138C>T NP_001269581.1:n.814-138C>T
NM_001282653.1:c.601-138C>T NP_001269582.1:n.601-138C>T
NM_006819.2:c.673-138C>T NP_006810.1:n.673-138C>T
NM_001282653.2:c.601-138C>T NP_001269582.1:n.601-138C>T
NM_006819.3:c.673-138C>T MANE Select NP_006810.1:n.673-138C>T
NM_001282652.2:c.814-138C>T NP_001269581.1:n.814-138C>T