Canonical Allele Identifier: CA1969385829

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47437942G= , CM000673.2:g.47437942G=	GRCh38
NC_000011.9:g.47459493G= , CM000673.1:g.47459493G=	GRCh37
NC_000011.8:g.47416069G=	NCBI36
NG_008312.1:g.16238C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.*33C= MANE Select	ENSP00000298854.2:n.*33C=
ENST00000298854.6:c.*33C=	ENSP00000298854.2:n.*33C=
ENST00000352508.7:c.*33C=	ENSP00000298853.3:n.*33C=
ENST00000524487.5:c.*33C=	ENSP00000435551.2:n.*33C=
ENST00000528356.1:n.227C=
NM_005055.4:c.*33C=	NP_005046.2:n.*33C=
NM_032645.4:c.*33C=	NP_116034.2:n.*33C=
XM_005253042.2:c.*33C=	XP_005253099.1:n.*33C=
XM_005253043.2:c.*33C=	XP_005253100.1:n.*33C=
XM_011520252.1:c.1357C=	XP_011518554.1:p.His453=
XM_011520253.1:c.*33C=	XP_011518555.1:n.*33C=
XM_005253042.3:c.*33C=	XP_005253099.1:n.*33C=
XM_005253043.3:c.*33C=	XP_005253100.1:n.*33C=
NM_005055.5:c.*33C= MANE Select	NP_005046.2:n.*33C=
NM_032645.5:c.*33C=	NP_116034.2:n.*33C=