Canonical Allele Identifier: CA1969385832

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47437946_47437947delinsAG , CM000673.2:g.47437946_47437947delinsAG	GRCh38
NC_000011.9:g.47459497_47459498delinsAG , CM000673.1:g.47459497_47459498delinsAG	GRCh37
NC_000011.8:g.47416073_47416074delinsAG	NCBI36
NG_008312.1:g.16233_16234delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.*28_*29delinsCT MANE Select	ENSP00000298854.2:n.*28_*29delinsCT
ENST00000298854.6:c.*28_*29delinsCT	ENSP00000298854.2:n.*28_*29delinsCT
ENST00000352508.7:c.*28_*29delinsCT	ENSP00000298853.3:n.*28_*29delinsCT
ENST00000524487.5:c.*28_*29delinsCT	ENSP00000435551.2:n.*28_*29delinsCT
ENST00000528356.1:n.222_223delinsCT
NM_005055.4:c.*28_*29delinsCT	NP_005046.2:n.*28_*29delinsCT
NM_032645.4:c.*28_*29delinsCT	NP_116034.2:n.*28_*29delinsCT
XM_005253042.2:c.*28_*29delinsCT	XP_005253099.1:n.*28_*29delinsCT
XM_005253043.2:c.*28_*29delinsCT	XP_005253100.1:n.*28_*29delinsCT
XM_011520252.1:c.1352_1353delinsCT	XP_011518554.1:p.Pro451=
XM_011520253.1:c.*28_*29delinsCT	XP_011518555.1:n.*28_*29delinsCT
XM_005253042.3:c.*28_*29delinsCT	XP_005253099.1:n.*28_*29delinsCT
XM_005253043.3:c.*28_*29delinsCT	XP_005253100.1:n.*28_*29delinsCT
NM_005055.5:c.*28_*29delinsCT MANE Select	NP_005046.2:n.*28_*29delinsCT
NM_032645.5:c.*28_*29delinsCT	NP_116034.2:n.*28_*29delinsCT