Canonical Allele Identifier: CA474220372

Gene: RAPSN

Linked Data

• COSMIC: COSM336377
• MyVariant Identifiers: chr11:g.47470382C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47448830C>G , CM000673.2:g.47448830C>G	GRCh38
NC_000011.9:g.47470382C>G , CM000673.1:g.47470382C>G	GRCh37
NC_000011.8:g.47426958C>G	NCBI36
NG_008312.1:g.5349G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298854.7:c.135G>C MANE Select	ENSP00000298854.2:p.Val45=
ENST00000298854.6:c.135G>C	ENSP00000298854.2:p.Val45=
ENST00000352508.7:c.135G>C	ENSP00000298853.3:p.Val45=
ENST00000524487.5:c.135G>C	ENSP00000435551.2:p.Val45=
ENST00000529341.1:c.135G>C	ENSP00000431732.1:p.Val45=
NM_005055.4:c.135G>C	NP_005046.2:p.Val45=
NM_032645.4:c.135G>C	NP_116034.2:p.Val45=
XM_005253042.2:c.135G>C	XP_005253099.1:p.Val45=
XM_005253043.2:c.135G>C	XP_005253100.1:p.Val45=
XM_011520252.1:c.135G>C	XP_011518554.1:p.Val45=
XM_011520253.1:c.135G>C	XP_011518555.1:p.Val45=
XM_005253042.3:c.135G>C	XP_005253099.1:p.Val45=
XM_005253043.3:c.135G>C	XP_005253100.1:p.Val45=
NM_005055.5:c.135G>C MANE Select	NP_005046.2:p.Val45=
NM_032645.5:c.135G>C	NP_116034.2:p.Val45=