Canonical Allele Identifier: CA380325406

Gene: RAPSN

Linked Data

• MyVariant Identifiers: chr11:g.47459542T>G (hg19) ; chr11:g.47437991T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47437991T>G , CM000673.2:g.47437991T>G	GRCh38
NC_000011.9:g.47459542T>G , CM000673.1:g.47459542T>G	GRCh37
NC_000011.8:g.47416118T>G	NCBI36
NG_008312.1:g.16189A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.1223A>C MANE Select	ENSP00000298854.2:p.Lys408Thr
ENST00000298854.6:c.1223A>C	ENSP00000298854.2:p.Lys408Thr
ENST00000352508.7:c.1046A>C	ENSP00000298853.3:p.Lys349Thr
ENST00000524487.5:c.1064A>C	ENSP00000435551.2:p.Lys355Thr
ENST00000528356.1:n.178A>C
NM_005055.4:c.1223A>C	NP_005046.2:p.Lys408Thr
NM_032645.4:c.1046A>C	NP_116034.2:p.Lys349Thr
XM_005253042.2:c.1169A>C	XP_005253099.1:p.Lys390Thr
XM_005253043.2:c.1100A>C	XP_005253100.1:p.Lys367Thr
XM_011520252.1:c.1308A>C	XP_011518554.1:p.Glu436Asp
XM_011520253.1:c.1247A>C	XP_011518555.1:p.Lys416Thr
XM_005253042.3:c.1169A>C	XP_005253099.1:p.Lys390Thr
XM_005253043.3:c.1100A>C	XP_005253100.1:p.Lys367Thr
NM_005055.5:c.1223A>C MANE Select	NP_005046.2:p.Lys408Thr
NM_032645.5:c.1046A>C	NP_116034.2:p.Lys349Thr