Canonical Allele Identifier: CA1198721090
Gene: RNF115 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.145790100A= , CM000663.2:g.145790100A= GRCh38
NC_000001.10:g.145644981T= , CM000663.1:g.145644981T= GRCh37
NC_000001.9:g.144356338T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000582693.5:c.103-1134T= MANE Select ENSP00000463650.1:n.103-1134T=
ENST00000582693.4:c.103-1134T= ENSP00000463650.1:n.103-1134T=
NM_014455.3:c.103-1134T= NP_055270.1:n.103-1134T=
XM_005272952.3:c.-49-1134T= XP_005273009.1:n.-49-1134T=
XM_011509419.1:c.103-1134T= XP_011507721.1:n.103-1134T=
XM_005272952.5:c.-49-1134T= XP_005273009.1:n.-49-1134T=
XR_001737118.2:n.302-1134T=
NM_014455.4:c.103-1134T= MANE Select NP_055270.1:n.103-1134T=
Search 100 bp 5'
Search 100 bp 3'