Canonical Allele Identifier: CA380325386

Gene: RAPSN

Linked Data

• MyVariant Identifiers: chr11:g.47459539G>C (hg19) ; chr11:g.47437988G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47437988G>C , CM000673.2:g.47437988G>C	GRCh38
NC_000011.9:g.47459539G>C , CM000673.1:g.47459539G>C	GRCh37
NC_000011.8:g.47416115G>C	NCBI36
NG_008312.1:g.16192C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.1226C>G MANE Select	ENSP00000298854.2:p.Pro409Arg
ENST00000298854.6:c.1226C>G	ENSP00000298854.2:p.Pro409Arg
ENST00000352508.7:c.1049C>G	ENSP00000298853.3:p.Pro350Arg
ENST00000524487.5:c.1067C>G	ENSP00000435551.2:p.Pro356Arg
ENST00000528356.1:n.181C>G
NM_005055.4:c.1226C>G	NP_005046.2:p.Pro409Arg
NM_032645.4:c.1049C>G	NP_116034.2:p.Pro350Arg
XM_005253042.2:c.1172C>G	XP_005253099.1:p.Pro391Arg
XM_005253043.2:c.1103C>G	XP_005253100.1:p.Pro368Arg
XM_011520252.1:c.1311C>G	XP_011518554.1:p.Ala437=
XM_011520253.1:c.1250C>G	XP_011518555.1:p.Pro417Arg
XM_005253042.3:c.1172C>G	XP_005253099.1:p.Pro391Arg
XM_005253043.3:c.1103C>G	XP_005253100.1:p.Pro368Arg
NM_005055.5:c.1226C>G MANE Select	NP_005046.2:p.Pro409Arg
NM_032645.5:c.1049C>G	NP_116034.2:p.Pro350Arg