Canonical Allele Identifier: CA1435976554

Gene: S100P

Linked Data

• dbSNP Id: rs1714363572

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6695940G>T , CM000666.2:g.6695940G>T	GRCh38
NC_000004.11:g.6697667G>T , CM000666.1:g.6697667G>T	GRCh37
NC_000004.10:g.6748568G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296370.4:c.139-953G>T MANE Select	ENSP00000296370.3:n.139-953G>T
ENST00000296370.3:c.139-953G>T	ENSP00000296370.3:n.139-953G>T
ENST00000513778.1:n.36-953G>T
NM_005980.2:c.139-953G>T	NP_005971.1:n.139-953G>T
NM_005980.3:c.139-953G>T MANE Select	NP_005971.1:n.139-953G>T