Canonical Allele Identifier: CA1198721104
Gene: RNF115 HGNC NCBI

Linked Data

dbSNP Id: rs1437007542

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.145790123dup , CM000663.2:g.145790123dup GRCh38
NC_000001.10:g.145644964dup , CM000663.1:g.145644964dup GRCh37
NC_000001.9:g.144356321dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000582693.5:c.103-1151dup MANE Select ENSP00000463650.1:n.103-1151dup
ENST00000582693.4:c.103-1151dup ENSP00000463650.1:n.103-1151dup
NM_014455.3:c.103-1151dup NP_055270.1:n.103-1151dup
XM_005272952.3:c.-49-1151dup XP_005273009.1:n.-49-1151dup
XM_011509419.1:c.103-1151dup XP_011507721.1:n.103-1151dup
XM_005272952.5:c.-49-1151dup XP_005273009.1:n.-49-1151dup
XR_001737118.2:n.302-1151dup
NM_014455.4:c.103-1151dup MANE Select NP_055270.1:n.103-1151dup