Canonical Allele Identifier: CA2739360158

Gene: RAPSN

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47441577A>C , CM000673.2:g.47441577A>C	GRCh38
NC_000011.9:g.47463129A>C , CM000673.1:g.47463129A>C	GRCh37
NC_000011.8:g.47419705A>C	NCBI36
NG_008312.1:g.12602T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298854.7:c.912+34T>G MANE Select	ENSP00000298854.2:n.912+34T>G
ENST00000298854.6:c.912+34T>G	ENSP00000298854.2:n.912+34T>G
ENST00000352508.7:c.789+246T>G	ENSP00000298853.3:n.789+246T>G
ENST00000524487.5:c.753+34T>G	ENSP00000435551.2:n.753+34T>G
ENST00000528356.1:n.121+34T>G
ENST00000529341.1:c.789+246T>G	ENSP00000431732.1:n.789+246T>G
NM_005055.4:c.912+34T>G	NP_005046.2:n.912+34T>G
NM_032645.4:c.789+246T>G	NP_116034.2:n.789+246T>G
XM_005253042.2:c.912+34T>G	XP_005253099.1:n.912+34T>G
XM_005253043.2:c.789+246T>G	XP_005253100.1:n.789+246T>G
XM_011520252.1:c.912+34T>G	XP_011518554.1:n.912+34T>G
XM_011520253.1:c.912+34T>G	XP_011518555.1:n.912+34T>G
XM_005253042.3:c.912+34T>G	XP_005253099.1:n.912+34T>G
XM_005253043.3:c.789+246T>G	XP_005253100.1:n.789+246T>G
NM_005055.5:c.912+34T>G MANE Select	NP_005046.2:n.912+34T>G
NM_032645.5:c.789+246T>G	NP_116034.2:n.789+246T>G