Canonical Allele Identifier: CA2574817065

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47437948G>A , CM000673.2:g.47437948G>A	GRCh38
NC_000011.9:g.47459499G>A , CM000673.1:g.47459499G>A	GRCh37
NC_000011.8:g.47416075G>A	NCBI36
NG_008312.1:g.16232C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.*27C>T MANE Select	ENSP00000298854.2:n.*27C>T
ENST00000298854.6:c.*27C>T	ENSP00000298854.2:n.*27C>T
ENST00000352508.7:c.*27C>T	ENSP00000298853.3:n.*27C>T
ENST00000524487.5:c.*27C>T	ENSP00000435551.2:n.*27C>T
ENST00000528356.1:n.221C>T
NM_005055.4:c.*27C>T	NP_005046.2:n.*27C>T
NM_032645.4:c.*27C>T	NP_116034.2:n.*27C>T
XM_005253042.2:c.*27C>T	XP_005253099.1:n.*27C>T
XM_005253043.2:c.*27C>T	XP_005253100.1:n.*27C>T
XM_011520252.1:c.1351C>T	XP_011518554.1:p.Pro451Ser
XM_011520253.1:c.*27C>T	XP_011518555.1:n.*27C>T
XM_005253042.3:c.*27C>T	XP_005253099.1:n.*27C>T
XM_005253043.3:c.*27C>T	XP_005253100.1:n.*27C>T
NM_005055.5:c.*27C>T MANE Select	NP_005046.2:n.*27C>T
NM_032645.5:c.*27C>T	NP_116034.2:n.*27C>T