Canonical Allele Identifier: CA677014838

Gene: RAPSN

Linked Data

• dbSNP Id: rs1418536513
• MyVariant Identifiers: chr11:g.47470281_47470282insC (hg19) ; chr11:g.47448729_47448730insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47448733dup , CM000673.2:g.47448733dup	GRCh38
NC_000011.9:g.47470285dup , CM000673.1:g.47470285dup	GRCh37
NC_000011.8:g.47426861dup	NCBI36
NG_008312.1:g.5449dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000298854.7:c.192+43dup MANE Select	ENSP00000298854.2:n.192+43dup
ENST00000298854.6:c.192+43dup	ENSP00000298854.2:n.192+43dup
ENST00000352508.7:c.192+43dup	ENSP00000298853.3:n.192+43dup
ENST00000524487.5:c.192+43dup	ENSP00000435551.2:n.192+43dup
ENST00000529341.1:c.192+43dup	ENSP00000431732.1:n.192+43dup
NM_005055.4:c.192+43dup	NP_005046.2:n.192+43dup
NM_032645.4:c.192+43dup	NP_116034.2:n.192+43dup
XM_005253042.2:c.192+43dup	XP_005253099.1:n.192+43dup
XM_005253043.2:c.192+43dup	XP_005253100.1:n.192+43dup
XM_011520252.1:c.192+43dup	XP_011518554.1:n.192+43dup
XM_011520253.1:c.192+43dup	XP_011518555.1:n.192+43dup
XM_005253042.3:c.192+43dup	XP_005253099.1:n.192+43dup
XM_005253043.3:c.192+43dup	XP_005253100.1:n.192+43dup
NM_005055.5:c.192+43dup MANE Select	NP_005046.2:n.192+43dup
NM_032645.5:c.192+43dup	NP_116034.2:n.192+43dup