Canonical Allele Identifier: CA1969387682

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47441828G= , CM000673.2:g.47441828G=	GRCh38
NC_000011.9:g.47463380G= , CM000673.1:g.47463380G=	GRCh37
NC_000011.8:g.47419956G=	NCBI36
NG_008312.1:g.12351C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.784C= MANE Select	ENSP00000298854.2:p.Leu262=
ENST00000298854.6:c.784C=	ENSP00000298854.2:p.Leu262=
ENST00000352508.7:c.784C=	ENSP00000298853.3:p.Leu262=
ENST00000524487.5:c.625C=	ENSP00000435551.2:p.Leu209=
ENST00000529341.1:c.784C=	ENSP00000431732.1:p.Leu262=
NM_005055.4:c.784C=	NP_005046.2:p.Leu262=
NM_032645.4:c.784C=	NP_116034.2:p.Leu262=
XM_005253042.2:c.784C=	XP_005253099.1:p.Leu262=
XM_005253043.2:c.784C=	XP_005253100.1:p.Leu262=
XM_011520252.1:c.784C=	XP_011518554.1:p.Leu262=
XM_011520253.1:c.784C=	XP_011518555.1:p.Leu262=
XM_005253042.3:c.784C=	XP_005253099.1:p.Leu262=
XM_005253043.3:c.784C=	XP_005253100.1:p.Leu262=
NM_005055.5:c.784C= MANE Select	NP_005046.2:p.Leu262=
NM_032645.5:c.784C=	NP_116034.2:p.Leu262=