Canonical Allele Identifier: CA1969388111
Gene: RAPSN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47442780G= , CM000673.2:g.47442780G= GRCh38
NC_000011.9:g.47464332G= , CM000673.1:g.47464332G= GRCh37
NC_000011.8:g.47420908G= NCBI36
NG_008312.1:g.11399C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298854.7:c.566C= MANE Select ENSP00000298854.2:p.Ala189=
ENST00000298854.6:c.566C= ENSP00000298854.2:p.Ala189=
ENST00000352508.7:c.566C= ENSP00000298853.3:p.Ala189=
ENST00000524487.5:c.532-859C= ENSP00000435551.2:n.532-859C=
ENST00000529341.1:c.566C= ENSP00000431732.1:p.Ala189=
NM_005055.4:c.566C= NP_005046.2:p.Ala189=
NM_032645.4:c.566C= NP_116034.2:p.Ala189=
XM_005253042.2:c.566C= XP_005253099.1:p.Ala189=
XM_005253043.2:c.566C= XP_005253100.1:p.Ala189=
XM_011520252.1:c.566C= XP_011518554.1:p.Ala189=
XM_011520253.1:c.566C= XP_011518555.1:p.Ala189=
XM_005253042.3:c.566C= XP_005253099.1:p.Ala189=
XM_005253043.3:c.566C= XP_005253100.1:p.Ala189=
NM_005055.5:c.566C= MANE Select NP_005046.2:p.Ala189=
NM_032645.5:c.566C= NP_116034.2:p.Ala189=