Canonical Allele Identifier: CA380329492

Gene: RAPSN

Linked Data

• MyVariant Identifiers: chr11:g.47463239A>G (hg19) ; chr11:g.47441687A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47441687A>G , CM000673.2:g.47441687A>G	GRCh38
NC_000011.9:g.47463239A>G , CM000673.1:g.47463239A>G	GRCh37
NC_000011.8:g.47419815A>G	NCBI36
NG_008312.1:g.12492T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298854.7:c.836T>C MANE Select	ENSP00000298854.2:p.Ile279Thr
ENST00000298854.6:c.836T>C	ENSP00000298854.2:p.Ile279Thr
ENST00000352508.7:c.789+136T>C	ENSP00000298853.3:n.789+136T>C
ENST00000524487.5:c.677T>C	ENSP00000435551.2:p.Ile226Thr
ENST00000528356.1:n.45T>C
ENST00000529341.1:c.789+136T>C	ENSP00000431732.1:n.789+136T>C
NM_005055.4:c.836T>C	NP_005046.2:p.Ile279Thr
NM_032645.4:c.789+136T>C	NP_116034.2:n.789+136T>C
XM_005253042.2:c.836T>C	XP_005253099.1:p.Ile279Thr
XM_005253043.2:c.789+136T>C	XP_005253100.1:n.789+136T>C
XM_011520252.1:c.836T>C	XP_011518554.1:p.Ile279Thr
XM_011520253.1:c.836T>C	XP_011518555.1:p.Ile279Thr
XM_005253042.3:c.836T>C	XP_005253099.1:p.Ile279Thr
XM_005253043.3:c.789+136T>C	XP_005253100.1:n.789+136T>C
NM_005055.5:c.836T>C MANE Select	NP_005046.2:p.Ile279Thr
NM_032645.5:c.789+136T>C	NP_116034.2:n.789+136T>C