Canonical Allele Identifier: CA1969385835

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47437958A= , CM000673.2:g.47437958A=	GRCh38
NC_000011.9:g.47459509A= , CM000673.1:g.47459509A=	GRCh37
NC_000011.8:g.47416085A=	NCBI36
NG_008312.1:g.16222T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.*17T= MANE Select	ENSP00000298854.2:n.*17T=
ENST00000298854.6:c.*17T=	ENSP00000298854.2:n.*17T=
ENST00000352508.7:c.*17T=	ENSP00000298853.3:n.*17T=
ENST00000524487.5:c.*17T=	ENSP00000435551.2:n.*17T=
ENST00000528356.1:n.211T=
NM_005055.4:c.*17T=	NP_005046.2:n.*17T=
NM_032645.4:c.*17T=	NP_116034.2:n.*17T=
XM_005253042.2:c.*17T=	XP_005253099.1:n.*17T=
XM_005253043.2:c.*17T=	XP_005253100.1:n.*17T=
XM_011520252.1:c.1341T=	XP_011518554.1:p.Arg447=
XM_011520253.1:c.*17T=	XP_011518555.1:n.*17T=
XM_005253042.3:c.*17T=	XP_005253099.1:n.*17T=
XM_005253043.3:c.*17T=	XP_005253100.1:n.*17T=
NM_005055.5:c.*17T= MANE Select	NP_005046.2:n.*17T=
NM_032645.5:c.*17T=	NP_116034.2:n.*17T=