Canonical Allele Identifier: CA380329013

Gene: RAPSN

Linked Data

• ClinVar Variation Id: 2952882
• ClinVar RCV Id: RCV003818016
• gnomAD v4: 11-47441638-G-T
• MyVariant Identifiers: chr11:g.47463190G>T (hg19) ; chr11:g.47441638G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47441638G>T , CM000673.2:g.47441638G>T	GRCh38
NC_000011.9:g.47463190G>T , CM000673.1:g.47463190G>T	GRCh37
NC_000011.8:g.47419766G>T	NCBI36
NG_008312.1:g.12541C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.885C>A MANE Select	ENSP00000298854.2:p.Cys295Ter
ENST00000298854.6:c.885C>A	ENSP00000298854.2:p.Cys295Ter
ENST00000352508.7:c.789+185C>A	ENSP00000298853.3:n.789+185C>A
ENST00000524487.5:c.726C>A	ENSP00000435551.2:p.Cys242Ter
ENST00000528356.1:n.94C>A
ENST00000529341.1:c.789+185C>A	ENSP00000431732.1:n.789+185C>A
NM_005055.4:c.885C>A	NP_005046.2:p.Cys295Ter
NM_032645.4:c.789+185C>A	NP_116034.2:n.789+185C>A
XM_005253042.2:c.885C>A	XP_005253099.1:p.Cys295Ter
XM_005253043.2:c.789+185C>A	XP_005253100.1:n.789+185C>A
XM_011520252.1:c.885C>A	XP_011518554.1:p.Cys295Ter
XM_011520253.1:c.885C>A	XP_011518555.1:p.Cys295Ter
XM_005253042.3:c.885C>A	XP_005253099.1:p.Cys295Ter
XM_005253043.3:c.789+185C>A	XP_005253100.1:n.789+185C>A
NM_005055.5:c.885C>A MANE Select	NP_005046.2:p.Cys295Ter
NM_032645.5:c.789+185C>A	NP_116034.2:n.789+185C>A