Canonical Allele Identifier: CA1969387579

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47441667C= , CM000673.2:g.47441667C=	GRCh38
NC_000011.9:g.47463219C= , CM000673.1:g.47463219C=	GRCh37
NC_000011.8:g.47419795C=	NCBI36
NG_008312.1:g.12512G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.856G= MANE Select	ENSP00000298854.2:p.Val286=
ENST00000298854.6:c.856G=	ENSP00000298854.2:p.Val286=
ENST00000352508.7:c.789+156G=	ENSP00000298853.3:n.789+156G=
ENST00000524487.5:c.697G=	ENSP00000435551.2:p.Val233=
ENST00000528356.1:n.65G=
ENST00000529341.1:c.789+156G=	ENSP00000431732.1:n.789+156G=
NM_005055.4:c.856G=	NP_005046.2:p.Val286=
NM_032645.4:c.789+156G=	NP_116034.2:n.789+156G=
XM_005253042.2:c.856G=	XP_005253099.1:p.Val286=
XM_005253043.2:c.789+156G=	XP_005253100.1:n.789+156G=
XM_011520252.1:c.856G=	XP_011518554.1:p.Val286=
XM_011520253.1:c.856G=	XP_011518555.1:p.Val286=
XM_005253042.3:c.856G=	XP_005253099.1:p.Val286=
XM_005253043.3:c.789+156G=	XP_005253100.1:n.789+156G=
NM_005055.5:c.856G= MANE Select	NP_005046.2:p.Val286=
NM_032645.5:c.789+156G=	NP_116034.2:n.789+156G=