Canonical Allele Identifier: CA2563254536

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47441747dup , CM000673.2:g.47441747dup	GRCh38
NC_000011.9:g.47463299dup , CM000673.1:g.47463299dup	GRCh37
NC_000011.8:g.47419875dup	NCBI36
NG_008312.1:g.12432dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.790-14dup MANE Select	ENSP00000298854.2:n.790-14dup
ENST00000298854.6:c.790-14dup	ENSP00000298854.2:n.790-14dup
ENST00000352508.7:c.789+76dup	ENSP00000298853.3:n.789+76dup
ENST00000524487.5:c.631-14dup	ENSP00000435551.2:n.631-14dup
ENST00000529341.1:c.789+76dup	ENSP00000431732.1:n.789+76dup
NM_005055.4:c.790-14dup	NP_005046.2:n.790-14dup
NM_032645.4:c.789+76dup	NP_116034.2:n.789+76dup
XM_005253042.2:c.790-14dup	XP_005253099.1:n.790-14dup
XM_005253043.2:c.789+76dup	XP_005253100.1:n.789+76dup
XM_011520252.1:c.790-14dup	XP_011518554.1:n.790-14dup
XM_011520253.1:c.790-14dup	XP_011518555.1:n.790-14dup
XM_005253042.3:c.790-14dup	XP_005253099.1:n.790-14dup
XM_005253043.3:c.789+76dup	XP_005253100.1:n.789+76dup
NM_005055.5:c.790-14dup MANE Select	NP_005046.2:n.790-14dup
NM_032645.5:c.789+76dup	NP_116034.2:n.789+76dup