Canonical Allele Identifier: CA13443241
Gene: STIP1 HGNC NCBI

Linked Data

dbSNP Id: rs2282490

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64194680T>C , CM000673.2:g.64194680T>C GRCh38
NC_000011.9:g.63962152T>C , CM000673.1:g.63962152T>C GRCh37
NC_000011.8:g.63718728T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000305218.9:c.503+60T>C MANE Select ENSP00000305958.5:n.503+60T>C
ENST00000305218.8:c.503+60T>C ENSP00000305958.4:n.503+60T>C
ENST00000358794.9:c.644+60T>C ENSP00000351646.5:n.644+60T>C
ENST00000536973.5:c.361+350T>C ENSP00000441036.1:n.361+350T>C
ENST00000538945.5:c.431+60T>C ENSP00000445957.1:n.431+60T>C
ENST00000540501.1:n.713+60T>C
ENST00000543847.1:c.503+60T>C ENSP00000442704.1:n.503+60T>C
NM_001282652.1:c.644+60T>C NP_001269581.1:n.644+60T>C
NM_001282653.1:c.431+60T>C NP_001269582.1:n.431+60T>C
NM_006819.2:c.503+60T>C NP_006810.1:n.503+60T>C
NM_001282653.2:c.431+60T>C NP_001269582.1:n.431+60T>C
NM_006819.3:c.503+60T>C MANE Select NP_006810.1:n.503+60T>C
NM_001282652.2:c.644+60T>C NP_001269581.1:n.644+60T>C