Canonical Allele Identifier: CA10813564
Gene: RAP1A HGNC NCBI
KRT18P57 HGNC NCBI

Linked Data

dbSNP Id: rs494453
gnomAD v2: 1-112192122-T-C
gnomAD v3: 1-111649500-T-C
gnomAD v4: 1-111649500-T-C
MyVariant Identifiers: chr1:g.112192122T>C (hg19) chr1:g.111649500T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.111649500T>C , CM000663.2:g.111649500T>C GRCh38
NC_000001.10:g.112192122T>C , CM000663.1:g.112192122T>C GRCh37
NC_000001.9:g.111993645T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369709.4:c.-28+29566T>C (RAP1A) MANE Select ENSP00000358723.3:n.-28+29566T>C
ENST00000687939.1:c.-28+21937T>C (RAP1A) ENSP00000509234.1:n.-28+21937T>C
ENST00000356415.5:c.-27-41834T>C (RAP1A) ENSP00000348786.1:n.-27-41834T>C
ENST00000369709.3:c.-28+29566T>C (RAP1A) ENSP00000358723.3:n.-28+29566T>C
ENST00000433097.5:c.-28+21937T>C (RAP1A) ENSP00000396741.1:n.-28+21937T>C
ENST00000443599.2:n.45A>G (KRT18P57)
ENST00000494982.1:n.91+21941T>C (RAP1A)
NM_001010935.2:c.-28+21937T>C (RAP1A) NP_001010935.1:n.-28+21937T>C
NM_001291896.1:c.-28+29153T>C (RAP1A) NP_001278825.1:n.-28+29153T>C
NM_002884.3:c.-28+29566T>C (RAP1A) NP_002875.1:n.-28+29566T>C
XM_017001961.1:c.-28+29153T>C (RAP1A) XP_016857450.1:n.-28+29153T>C
XM_017001962.1:c.-28+21937T>C (RAP1A) XP_016857451.1:n.-28+21937T>C
XM_017001964.1:c.-27-41834T>C (RAP1A) XP_016857453.1:n.-27-41834T>C
XM_024448786.1:c.-28+21937T>C (RAP1A) XP_024304554.1:n.-28+21937T>C
XR_946724.2:n.24+21937T>C (RAP1A)
NM_001370216.1:c.-27-41834T>C (RAP1A) NP_001357145.1:n.-27-41834T>C
NM_001010935.3:c.-28+21937T>C (RAP1A) NP_001010935.1:n.-28+21937T>C
NM_001291896.3:c.-28+29153T>C (RAP1A) NP_001278825.1:n.-28+29153T>C
NM_001370216.2:c.-27-41834T>C (RAP1A) NP_001357145.1:n.-27-41834T>C
NM_001370217.2:c.-107-15292T>C (RAP1A) NP_001357146.1:n.-107-15292T>C
NM_001394066.1:c.-107-15292T>C (RAP1A) NP_001380995.1:n.-107-15292T>C
NM_002884.4:c.-28+29566T>C (RAP1A) MANE Select NP_002875.1:n.-28+29566T>C
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