Canonical Allele Identifier: CA2739360029

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47437905A>T , CM000673.2:g.47437905A>T	GRCh38
NC_000011.9:g.47459456A>T , CM000673.1:g.47459456A>T	GRCh37
NC_000011.8:g.47416032A>T	NCBI36
NG_008312.1:g.16275T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.*70T>A MANE Select	ENSP00000298854.2:n.*70T>A
ENST00000298854.6:c.*70T>A	ENSP00000298854.2:n.*70T>A
ENST00000352508.7:c.*70T>A	ENSP00000298853.3:n.*70T>A
ENST00000524487.5:c.*70T>A	ENSP00000435551.2:n.*70T>A
ENST00000528356.1:n.264T>A
NM_005055.4:c.*70T>A	NP_005046.2:n.*70T>A
NM_032645.4:c.*70T>A	NP_116034.2:n.*70T>A
XM_005253042.2:c.*70T>A	XP_005253099.1:n.*70T>A
XM_005253043.2:c.*70T>A	XP_005253100.1:n.*70T>A
XM_011520252.1:c.1394T>A	XP_011518554.1:p.Ile465Asn
XM_011520253.1:c.*70T>A	XP_011518555.1:n.*70T>A
XM_005253042.3:c.*70T>A	XP_005253099.1:n.*70T>A
XM_005253043.3:c.*70T>A	XP_005253100.1:n.*70T>A
NM_005055.5:c.*70T>A MANE Select	NP_005046.2:n.*70T>A
NM_032645.5:c.*70T>A	NP_116034.2:n.*70T>A