Canonical Allele Identifier: CA2739359922
Gene: RAPSN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47437822A>T , CM000673.2:g.47437822A>T GRCh38
NC_000011.9:g.47459373A>T , CM000673.1:g.47459373A>T GRCh37
NC_000011.8:g.47415949A>T NCBI36
NG_008312.1:g.16358T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298854.7:c.*153T>A MANE Select ENSP00000298854.2:n.*153T>A
ENST00000298854.6:c.*153T>A ENSP00000298854.2:n.*153T>A
ENST00000352508.7:c.*153T>A ENSP00000298853.3:n.*153T>A
ENST00000524487.5:c.*153T>A ENSP00000435551.2:n.*153T>A
ENST00000528356.1:n.347T>A
NM_005055.4:c.*153T>A NP_005046.2:n.*153T>A
NM_032645.4:c.*153T>A NP_116034.2:n.*153T>A
XM_011520252.1:c.1477T>A XP_011518554.1:p.Ser493Thr
NM_005055.5:c.*153T>A MANE Select NP_005046.2:n.*153T>A
NM_032645.5:c.*153T>A NP_116034.2:n.*153T>A
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