Canonical Allele Identifier: CA420234312

Gene: RNF115

Linked Data

• dbSNP Id: rs587661571
• gnomAD v3: 1-145790103-T-C
• gnomAD v4: 1-145790103-T-C
• MyVariant Identifiers: chr1:g.145644978A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.145790103T>C , CM000663.2:g.145790103T>C	GRCh38
NC_000001.10:g.145644978A>G , CM000663.1:g.145644978A>G	GRCh37
NC_000001.9:g.144356335A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000582693.5:c.103-1137A>G MANE Select	ENSP00000463650.1:n.103-1137A>G
ENST00000582693.4:c.103-1137A>G	ENSP00000463650.1:n.103-1137A>G
NM_014455.3:c.103-1137A>G	NP_055270.1:n.103-1137A>G
XM_005272952.3:c.-49-1137A>G	XP_005273009.1:n.-49-1137A>G
XM_011509419.1:c.103-1137A>G	XP_011507721.1:n.103-1137A>G
XM_005272952.5:c.-49-1137A>G	XP_005273009.1:n.-49-1137A>G
XR_001737118.2:n.302-1137A>G
NM_014455.4:c.103-1137A>G MANE Select	NP_055270.1:n.103-1137A>G