Canonical Allele Identifier: CA1198721106

Gene: RNF115

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.145790119T= , CM000663.2:g.145790119T=	GRCh38
NC_000001.10:g.145644962A= , CM000663.1:g.145644962A=	GRCh37
NC_000001.9:g.144356319A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000582693.5:c.103-1153A= MANE Select	ENSP00000463650.1:n.103-1153A=
ENST00000582693.4:c.103-1153A=	ENSP00000463650.1:n.103-1153A=
NM_014455.3:c.103-1153A=	NP_055270.1:n.103-1153A=
XM_005272952.3:c.-49-1153A=	XP_005273009.1:n.-49-1153A=
XM_011509419.1:c.103-1153A=	XP_011507721.1:n.103-1153A=
XM_005272952.5:c.-49-1153A=	XP_005273009.1:n.-49-1153A=
XR_001737118.2:n.302-1153A=
NM_014455.4:c.103-1153A= MANE Select	NP_055270.1:n.103-1153A=