Canonical Allele Identifier: CA1969385791

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47437856C= , CM000673.2:g.47437856C=	GRCh38
NC_000011.9:g.47459407C= , CM000673.1:g.47459407C=	GRCh37
NC_000011.8:g.47415983C=	NCBI36
NG_008312.1:g.16324G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.*119G= MANE Select	ENSP00000298854.2:n.*119G=
ENST00000298854.6:c.*119G=	ENSP00000298854.2:n.*119G=
ENST00000352508.7:c.*119G=	ENSP00000298853.3:n.*119G=
ENST00000524487.5:c.*119G=	ENSP00000435551.2:n.*119G=
ENST00000528356.1:n.313G=
NM_005055.4:c.*119G=	NP_005046.2:n.*119G=
NM_032645.4:c.*119G=	NP_116034.2:n.*119G=
XM_011520252.1:c.1443G=	XP_011518554.1:p.Leu481=
NM_005055.5:c.*119G= MANE Select	NP_005046.2:n.*119G=
NM_032645.5:c.*119G=	NP_116034.2:n.*119G=