Canonical Allele Identifier: CA916263157
Gene: RAP1A HGNC NCBI

Linked Data

dbSNP Id: rs1557852312

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111564886del , CM000663.2:g.111564886del GRCh38
NC_000001.10:g.112107508del , CM000663.1:g.112107508del GRCh37
NC_000001.9:g.111909031del NCBI36
NG_032119.1:g.4095del , LRG_424:g.4095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000356415.5:c.-28+22377del ENSP00000348786.1:n.-28+22377del
XM_017001964.1:c.-28+22377del XP_016857453.1:n.-28+22377del
NM_001370216.1:c.-28+22377del NP_001357145.1:n.-28+22377del
NM_001370216.2:c.-28+22377del NP_001357145.1:n.-28+22377del