Canonical Allele Identifier: CA15071086
Gene: RAP1A HGNC NCBI
INKA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111712767C>A , CM000663.2:g.111712767C>A GRCh38
NC_000001.10:g.112255389C>A , CM000663.1:g.112255389C>A GRCh37
NC_000001.9:g.112056912C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369709.4:c.*366C>A (RAP1A) MANE Select ENSP00000358723.3:n.*366C>A
ENST00000687939.1:c.*366C>A (RAP1A) ENSP00000509234.1:n.*366C>A
ENST00000356415.5:c.*366C>A (RAP1A) ENSP00000348786.1:n.*366C>A
ENST00000369709.3:c.*366C>A (RAP1A) ENSP00000358723.3:n.*366C>A
ENST00000527570.1:n.219-26084G>T (INKA2)
NM_001010935.2:c.*366C>A (RAP1A) NP_001010935.1:n.*366C>A
NM_001291896.1:c.*366C>A (RAP1A) NP_001278825.1:n.*366C>A
NM_002884.3:c.*366C>A (RAP1A) NP_002875.1:n.*366C>A
XR_946724.1:n.1086C>A (RAP1A)
XM_017001962.1:c.*366C>A (RAP1A) XP_016857451.1:n.*366C>A
XM_017001963.1:c.*366C>A (RAP1A) XP_016857452.1:n.*366C>A
XM_017001964.1:c.*366C>A (RAP1A) XP_016857453.1:n.*366C>A
XM_024448786.1:c.*366C>A (RAP1A) XP_024304554.1:n.*366C>A
XR_946724.2:n.1087C>A (RAP1A)
NM_001370216.1:c.*366C>A (RAP1A) NP_001357145.1:n.*366C>A
NM_001370217.1:c.*366C>A (RAP1A) NP_001357146.1:n.*366C>A
NM_001010935.3:c.*366C>A (RAP1A) NP_001010935.1:n.*366C>A
NM_001291896.3:c.*366C>A (RAP1A) NP_001278825.1:n.*366C>A
NM_001370216.2:c.*366C>A (RAP1A) NP_001357145.1:n.*366C>A
NM_001370217.2:c.*366C>A (RAP1A) NP_001357146.1:n.*366C>A
NM_001394066.1:c.*366C>A (RAP1A) NP_001380995.1:n.*366C>A
NM_002884.4:c.*366C>A (RAP1A) MANE Select NP_002875.1:n.*366C>A
Search 100 bp 5'
Search 100 bp 3'