Canonical Allele Identifier: CA380329687

Gene: RAPSN

Linked Data

• dbSNP Id: rs1026111662
• gnomAD v4: 11-47441705-A-G
• MyVariant Identifiers: chr11:g.47463257A>G (hg19) ; chr11:g.47441705A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47441705A>G , CM000673.2:g.47441705A>G	GRCh38
NC_000011.9:g.47463257A>G , CM000673.1:g.47463257A>G	GRCh37
NC_000011.8:g.47419833A>G	NCBI36
NG_008312.1:g.12474T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.818T>C MANE Select	ENSP00000298854.2:p.Met273Thr
ENST00000298854.6:c.818T>C	ENSP00000298854.2:p.Met273Thr
ENST00000352508.7:c.789+118T>C	ENSP00000298853.3:n.789+118T>C
ENST00000524487.5:c.659T>C	ENSP00000435551.2:p.Met220Thr
ENST00000528356.1:n.27T>C
ENST00000529341.1:c.789+118T>C	ENSP00000431732.1:n.789+118T>C
NM_005055.4:c.818T>C	NP_005046.2:p.Met273Thr
NM_032645.4:c.789+118T>C	NP_116034.2:n.789+118T>C
XM_005253042.2:c.818T>C	XP_005253099.1:p.Met273Thr
XM_005253043.2:c.789+118T>C	XP_005253100.1:n.789+118T>C
XM_011520252.1:c.818T>C	XP_011518554.1:p.Met273Thr
XM_011520253.1:c.818T>C	XP_011518555.1:p.Met273Thr
XM_005253042.3:c.818T>C	XP_005253099.1:p.Met273Thr
XM_005253043.3:c.789+118T>C	XP_005253100.1:n.789+118T>C
NM_005055.5:c.818T>C MANE Select	NP_005046.2:p.Met273Thr
NM_032645.5:c.789+118T>C	NP_116034.2:n.789+118T>C