Canonical Allele Identifier: CA2581730900
Gene: RNF115 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.145790097G>T , CM000663.2:g.145790097G>T GRCh38
NC_000001.10:g.145644984C>A , CM000663.1:g.145644984C>A GRCh37
NC_000001.9:g.144356341C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000582693.5:c.103-1131C>A MANE Select ENSP00000463650.1:n.103-1131C>A
ENST00000582693.4:c.103-1131C>A ENSP00000463650.1:n.103-1131C>A
NM_014455.3:c.103-1131C>A NP_055270.1:n.103-1131C>A
XM_005272952.3:c.-49-1131C>A XP_005273009.1:n.-49-1131C>A
XM_011509419.1:c.103-1131C>A XP_011507721.1:n.103-1131C>A
XM_005272952.5:c.-49-1131C>A XP_005273009.1:n.-49-1131C>A
XR_001737118.2:n.302-1131C>A
NM_014455.4:c.103-1131C>A MANE Select NP_055270.1:n.103-1131C>A
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