Canonical Allele Identifier: CA380329296
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 1016297
ClinVar RCV Id: RCV001315283
dbSNP Id: rs1294627986

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47441673C>T , CM000673.2:g.47441673C>T GRCh38
NC_000011.9:g.47463225C>T , CM000673.1:g.47463225C>T GRCh37
NC_000011.8:g.47419801C>T NCBI36
NG_008312.1:g.12506G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298854.7:c.850G>A MANE Select ENSP00000298854.2:p.Gly284Arg
ENST00000298854.6:c.850G>A ENSP00000298854.2:p.Gly284Arg
ENST00000352508.7:c.789+150G>A ENSP00000298853.3:n.789+150G>A
ENST00000524487.5:c.691G>A ENSP00000435551.2:p.Gly231Arg
ENST00000528356.1:n.59G>A
ENST00000529341.1:c.789+150G>A ENSP00000431732.1:n.789+150G>A
NM_005055.4:c.850G>A NP_005046.2:p.Gly284Arg
NM_032645.4:c.789+150G>A NP_116034.2:n.789+150G>A
XM_005253042.2:c.850G>A XP_005253099.1:p.Gly284Arg
XM_005253043.2:c.789+150G>A XP_005253100.1:n.789+150G>A
XM_011520252.1:c.850G>A XP_011518554.1:p.Gly284Arg
XM_011520253.1:c.850G>A XP_011518555.1:p.Gly284Arg
XM_005253042.3:c.850G>A XP_005253099.1:p.Gly284Arg
XM_005253043.3:c.789+150G>A XP_005253100.1:n.789+150G>A
NM_005055.5:c.850G>A MANE Select NP_005046.2:p.Gly284Arg
NM_032645.5:c.789+150G>A NP_116034.2:n.789+150G>A