Canonical Allele Identifier: CA1435976626

Gene: S100P

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6696090_6696091delinsTG , CM000666.2:g.6696090_6696091delinsTG	GRCh38
NC_000004.11:g.6697817_6697818delinsTG , CM000666.1:g.6697817_6697818delinsTG	GRCh37
NC_000004.10:g.6748718_6748719delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296370.4:c.139-803_139-802delinsTG MANE Select	ENSP00000296370.3:n.139-803_139-802delinsTG
ENST00000296370.3:c.139-803_139-802delinsTG	ENSP00000296370.3:n.139-803_139-802delinsTG
ENST00000513778.1:n.36-803_36-802delinsTG
NM_005980.2:c.139-803_139-802delinsTG	NP_005971.1:n.139-803_139-802delinsTG
NM_005980.3:c.139-803_139-802delinsTG MANE Select	NP_005971.1:n.139-803_139-802delinsTG