Canonical Allele Identifier: CA380333737

Gene: RAPSN

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47447853G>C , CM000673.2:g.47447853G>C	GRCh38
NC_000011.9:g.47469405G>C , CM000673.1:g.47469405G>C	GRCh37
NC_000011.8:g.47425981G>C	NCBI36
NG_008312.1:g.6326C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.490C>G MANE Select	ENSP00000298854.2:p.Arg164Gly
ENST00000298854.6:c.490C>G	ENSP00000298854.2:p.Arg164Gly
ENST00000352508.7:c.490C>G	ENSP00000298853.3:p.Arg164Gly
ENST00000524487.5:c.490C>G	ENSP00000435551.2:p.Arg164Gly
ENST00000529341.1:c.490C>G	ENSP00000431732.1:p.Arg164Gly
NM_005055.4:c.490C>G	NP_005046.2:p.Arg164Gly
NM_032645.4:c.490C>G	NP_116034.2:p.Arg164Gly
XM_005253042.2:c.490C>G	XP_005253099.1:p.Arg164Gly
XM_005253043.2:c.490C>G	XP_005253100.1:p.Arg164Gly
XM_011520252.1:c.490C>G	XP_011518554.1:p.Arg164Gly
XM_011520253.1:c.490C>G	XP_011518555.1:p.Arg164Gly
XM_005253042.3:c.490C>G	XP_005253099.1:p.Arg164Gly
XM_005253043.3:c.490C>G	XP_005253100.1:p.Arg164Gly
NM_005055.5:c.490C>G MANE Select	NP_005046.2:p.Arg164Gly
NM_032645.5:c.490C>G	NP_116034.2:p.Arg164Gly