Canonical Allele Identifier: CA2531695901

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47449068_47449075del , CM000673.2:g.47449068_47449075del	GRCh38
NC_000011.9:g.47470620_47470627del , CM000673.1:g.47470620_47470627del	GRCh37
NC_000011.8:g.47427196_47427203del	NCBI36
NG_008312.1:g.5104_5111del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.-111_-104del MANE Select	ENSP00000298854.2:n.-111_-104del
ENST00000298854.6:c.-111_-104del	ENSP00000298854.2:n.-111_-104del
ENST00000352508.7:c.-111_-104del	ENSP00000298853.3:n.-111_-104del
ENST00000524487.5:c.-111_-104del	ENSP00000435551.2:n.-111_-104del
ENST00000529341.1:c.-111_-104del	ENSP00000431732.1:n.-111_-104del
NM_005055.4:c.-111_-104del	NP_005046.2:n.-111_-104del
NM_032645.4:c.-111_-104del	NP_116034.2:n.-111_-104del
XM_005253042.2:c.-111_-104del	XP_005253099.1:n.-111_-104del
XM_005253043.2:c.-111_-104del	XP_005253100.1:n.-111_-104del
XM_011520252.1:c.-111_-104del	XP_011518554.1:n.-111_-104del
XM_011520253.1:c.-111_-104del	XP_011518555.1:n.-111_-104del
XM_005253042.3:c.-111_-104del	XP_005253099.1:n.-111_-104del
XM_005253043.3:c.-111_-104del	XP_005253100.1:n.-111_-104del
NM_005055.5:c.-111_-104del MANE Select	NP_005046.2:n.-111_-104del
NM_032645.5:c.-111_-104del	NP_116034.2:n.-111_-104del