Canonical Allele Identifier: CA2549768723
Gene: S100P HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6696031G>C , CM000666.2:g.6696031G>C GRCh38
NC_000004.11:g.6697758G>C , CM000666.1:g.6697758G>C GRCh37
NC_000004.10:g.6748659G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296370.4:c.139-862G>C MANE Select ENSP00000296370.3:n.139-862G>C
ENST00000296370.3:c.139-862G>C ENSP00000296370.3:n.139-862G>C
ENST00000513778.1:n.36-862G>C
NM_005980.2:c.139-862G>C NP_005971.1:n.139-862G>C
NM_005980.3:c.139-862G>C MANE Select NP_005971.1:n.139-862G>C
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