Canonical Allele Identifier: CA1198721091

Gene: RNF115

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.145790100_145790101delinsAG , CM000663.2:g.145790100_145790101delinsAG	GRCh38
NC_000001.10:g.145644980_145644981delinsCT , CM000663.1:g.145644980_145644981delinsCT	GRCh37
NC_000001.9:g.144356337_144356338delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000582693.5:c.103-1135_103-1134delinsCT MANE Select	ENSP00000463650.1:n.103-1135_103-1134delinsCT
ENST00000582693.4:c.103-1135_103-1134delinsCT	ENSP00000463650.1:n.103-1135_103-1134delinsCT
NM_014455.3:c.103-1135_103-1134delinsCT	NP_055270.1:n.103-1135_103-1134delinsCT
XM_005272952.3:c.-49-1135_-49-1134delinsCT	XP_005273009.1:n.-49-1135_-49-1134delinsCT
XM_011509419.1:c.103-1135_103-1134delinsCT	XP_011507721.1:n.103-1135_103-1134delinsCT
XM_005272952.5:c.-49-1135_-49-1134delinsCT	XP_005273009.1:n.-49-1135_-49-1134delinsCT
XR_001737118.2:n.302-1135_302-1134delinsCT
NM_014455.4:c.103-1135_103-1134delinsCT MANE Select	NP_055270.1:n.103-1135_103-1134delinsCT