Canonical Allele Identifier: CA888519325

Gene: RNF115

Linked Data

• dbSNP Id: rs1437007542
• MyVariant Identifiers: chr1:g.145790117_145790120del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.145790120_145790123del , CM000663.2:g.145790120_145790123del	GRCh38
NC_000001.10:g.145644961_145644964del , CM000663.1:g.145644961_145644964del	GRCh37
NC_000001.9:g.144356318_144356321del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000582693.5:c.103-1154_103-1151del MANE Select	ENSP00000463650.1:n.103-1154_103-1151del
ENST00000582693.4:c.103-1154_103-1151del	ENSP00000463650.1:n.103-1154_103-1151del
NM_014455.3:c.103-1154_103-1151del	NP_055270.1:n.103-1154_103-1151del
XM_005272952.3:c.-49-1154_-49-1151del	XP_005273009.1:n.-49-1154_-49-1151del
XM_011509419.1:c.103-1154_103-1151del	XP_011507721.1:n.103-1154_103-1151del
XM_005272952.5:c.-49-1154_-49-1151del	XP_005273009.1:n.-49-1154_-49-1151del
XR_001737118.2:n.302-1154_302-1151del
NM_014455.4:c.103-1154_103-1151del MANE Select	NP_055270.1:n.103-1154_103-1151del