Canonical Allele Identifier: CA380328834
Gene: RAPSN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47441612T>A , CM000673.2:g.47441612T>A GRCh38
NC_000011.9:g.47463164T>A , CM000673.1:g.47463164T>A GRCh37
NC_000011.8:g.47419740T>A NCBI36
NG_008312.1:g.12567A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298854.7:c.911A>T MANE Select ENSP00000298854.2:p.Lys304Met
ENST00000298854.6:c.911A>T ENSP00000298854.2:p.Lys304Met
ENST00000352508.7:c.789+211A>T ENSP00000298853.3:n.789+211A>T
ENST00000524487.5:c.752A>T ENSP00000435551.2:p.Lys251Met
ENST00000528356.1:n.120A>T
ENST00000529341.1:c.789+211A>T ENSP00000431732.1:n.789+211A>T
NM_005055.4:c.911A>T NP_005046.2:p.Lys304Met
NM_032645.4:c.789+211A>T NP_116034.2:n.789+211A>T
XM_005253042.2:c.911A>T XP_005253099.1:p.Lys304Met
XM_005253043.2:c.789+211A>T XP_005253100.1:n.789+211A>T
XM_011520252.1:c.911A>T XP_011518554.1:p.Lys304Met
XM_011520253.1:c.911A>T XP_011518555.1:p.Lys304Met
XM_005253042.3:c.911A>T XP_005253099.1:p.Lys304Met
XM_005253043.3:c.789+211A>T XP_005253100.1:n.789+211A>T
NM_005055.5:c.911A>T MANE Select NP_005046.2:p.Lys304Met
NM_032645.5:c.789+211A>T NP_116034.2:n.789+211A>T