Canonical Allele Identifier: CA380328902

Gene: RAPSN

Linked Data

• MyVariant Identifiers: chr11:g.47463178C>G (hg19) ; chr11:g.47441626C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47441626C>G , CM000673.2:g.47441626C>G	GRCh38
NC_000011.9:g.47463178C>G , CM000673.1:g.47463178C>G	GRCh37
NC_000011.8:g.47419754C>G	NCBI36
NG_008312.1:g.12553G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.897G>C MANE Select	ENSP00000298854.2:p.Arg299Ser
ENST00000298854.6:c.897G>C	ENSP00000298854.2:p.Arg299Ser
ENST00000352508.7:c.789+197G>C	ENSP00000298853.3:n.789+197G>C
ENST00000524487.5:c.738G>C	ENSP00000435551.2:p.Arg246Ser
ENST00000528356.1:n.106G>C
ENST00000529341.1:c.789+197G>C	ENSP00000431732.1:n.789+197G>C
NM_005055.4:c.897G>C	NP_005046.2:p.Arg299Ser
NM_032645.4:c.789+197G>C	NP_116034.2:n.789+197G>C
XM_005253042.2:c.897G>C	XP_005253099.1:p.Arg299Ser
XM_005253043.2:c.789+197G>C	XP_005253100.1:n.789+197G>C
XM_011520252.1:c.897G>C	XP_011518554.1:p.Arg299Ser
XM_011520253.1:c.897G>C	XP_011518555.1:p.Arg299Ser
XM_005253042.3:c.897G>C	XP_005253099.1:p.Arg299Ser
XM_005253043.3:c.789+197G>C	XP_005253100.1:n.789+197G>C
NM_005055.5:c.897G>C MANE Select	NP_005046.2:p.Arg299Ser
NM_032645.5:c.789+197G>C	NP_116034.2:n.789+197G>C