Canonical Allele Identifier: CA1188974216
Gene: RAP1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111565004_111565012delinsGGGGTCTAT , CM000663.2:g.111565004_111565012delinsGGGGTCTAT GRCh38
NC_000001.10:g.112107626_112107634delinsGGGGTCTAT , CM000663.1:g.112107626_112107634delinsGGGGTCTAT GRCh37
NC_000001.9:g.111909149_111909157delinsGGGGTCTAT NCBI36
NG_032119.1:g.3964_3972delinsATAGACCCC , LRG_424:g.3964_3972delinsATAGACCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000356415.5:c.-28+22495_-28+22503delinsGGGGTCTAT ENSP00000348786.1:n.-28+22495_-28+22503delinsGGGGTCTAT
XM_017001964.1:c.-28+22495_-28+22503delinsGGGGTCTAT XP_016857453.1:n.-28+22495_-28+22503delinsGGGGTCTAT
NM_001370216.1:c.-28+22495_-28+22503delinsGGGGTCTAT NP_001357145.1:n.-28+22495_-28+22503delinsGGGGTCTAT
NM_001370216.2:c.-28+22495_-28+22503delinsGGGGTCTAT NP_001357145.1:n.-28+22495_-28+22503delinsGGGGTCTAT