Canonical Allele Identifier: CA1435976598
Gene: S100P HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6696030A= , CM000666.2:g.6696030A= GRCh38
NC_000004.11:g.6697757A= , CM000666.1:g.6697757A= GRCh37
NC_000004.10:g.6748658A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296370.4:c.139-863A= MANE Select ENSP00000296370.3:n.139-863A=
ENST00000296370.3:c.139-863A= ENSP00000296370.3:n.139-863A=
ENST00000513778.1:n.36-863A=
NM_005980.2:c.139-863A= NP_005971.1:n.139-863A=
NM_005980.3:c.139-863A= MANE Select NP_005971.1:n.139-863A=
Search 100 bp 5'
Search 100 bp 3'