Canonical Allele Identifier: CA2509686157
Gene: S100P HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6695964A>G , CM000666.2:g.6695964A>G GRCh38
NC_000004.11:g.6697691A>G , CM000666.1:g.6697691A>G GRCh37
NC_000004.10:g.6748592A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296370.4:c.139-929A>G MANE Select ENSP00000296370.3:n.139-929A>G
ENST00000296370.3:c.139-929A>G ENSP00000296370.3:n.139-929A>G
ENST00000513778.1:n.36-929A>G
NM_005980.2:c.139-929A>G NP_005971.1:n.139-929A>G
NM_005980.3:c.139-929A>G MANE Select NP_005971.1:n.139-929A>G
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