Canonical Allele Identifier: CA549436814

Gene: S100P

Linked Data

• dbSNP Id: rs1553813178
• gnomAD v2: 4-6697722-CCTTA-C
• gnomAD v3: 4-6695995-CCTTA-C
• gnomAD v4: 4-6695995-CCTTA-C
• MyVariant Identifiers: chr4:g.6697723_6697726del (hg19) ; chr4:g.6695996_6695999del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6695999_6696002del , CM000666.2:g.6695999_6696002del	GRCh38
NC_000004.11:g.6697726_6697729del , CM000666.1:g.6697726_6697729del	GRCh37
NC_000004.10:g.6748627_6748630del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296370.4:c.139-894_139-891del MANE Select	ENSP00000296370.3:n.139-894_139-891del
ENST00000296370.3:c.139-894_139-891del	ENSP00000296370.3:n.139-894_139-891del
ENST00000513778.1:n.36-894_36-891del
NM_005980.2:c.139-894_139-891del	NP_005971.1:n.139-894_139-891del
NM_005980.3:c.139-894_139-891del MANE Select	NP_005971.1:n.139-894_139-891del