Canonical Allele Identifier: CA1435976584

Gene: S100P

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6695989_6695990delinsTC , CM000666.2:g.6695989_6695990delinsTC	GRCh38
NC_000004.11:g.6697716_6697717delinsTC , CM000666.1:g.6697716_6697717delinsTC	GRCh37
NC_000004.10:g.6748617_6748618delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296370.4:c.139-904_139-903delinsTC MANE Select	ENSP00000296370.3:n.139-904_139-903delinsTC
ENST00000296370.3:c.139-904_139-903delinsTC	ENSP00000296370.3:n.139-904_139-903delinsTC
ENST00000513778.1:n.36-904_36-903delinsTC
NM_005980.2:c.139-904_139-903delinsTC	NP_005971.1:n.139-904_139-903delinsTC
NM_005980.3:c.139-904_139-903delinsTC MANE Select	NP_005971.1:n.139-904_139-903delinsTC