Canonical Allele Identifier: CA2604360128
Gene: RNF115 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.145790185G>A , CM000663.2:g.145790185G>A GRCh38
NC_000001.10:g.145644896C>T , CM000663.1:g.145644896C>T GRCh37
NC_000001.9:g.144356253C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000582693.5:c.103-1219C>T MANE Select ENSP00000463650.1:n.103-1219C>T
ENST00000582693.4:c.103-1219C>T ENSP00000463650.1:n.103-1219C>T
NM_014455.3:c.103-1219C>T NP_055270.1:n.103-1219C>T
XM_005272952.3:c.-49-1219C>T XP_005273009.1:n.-49-1219C>T
XM_011509419.1:c.103-1219C>T XP_011507721.1:n.103-1219C>T
XM_005272952.5:c.-49-1219C>T XP_005273009.1:n.-49-1219C>T
XR_001737118.2:n.302-1219C>T
NM_014455.4:c.103-1219C>T MANE Select NP_055270.1:n.103-1219C>T