Canonical Allele Identifier: CA2841234641
Gene: S100P HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6695945G>A , CM000666.2:g.6695945G>A GRCh38
NC_000004.11:g.6697672G>A , CM000666.1:g.6697672G>A GRCh37
NC_000004.10:g.6748573G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296370.4:c.139-948G>A MANE Select ENSP00000296370.3:n.139-948G>A
ENST00000296370.3:c.139-948G>A ENSP00000296370.3:n.139-948G>A
ENST00000513778.1:n.36-948G>A
NM_005980.2:c.139-948G>A NP_005971.1:n.139-948G>A
NM_005980.3:c.139-948G>A MANE Select NP_005971.1:n.139-948G>A
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