Canonical Allele Identifier: CA380325346

Gene: RAPSN

Linked Data

• MyVariant Identifiers: chr11:g.47459530A>G (hg19) ; chr11:g.47437979A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47437979A>G , CM000673.2:g.47437979A>G	GRCh38
NC_000011.9:g.47459530A>G , CM000673.1:g.47459530A>G	GRCh37
NC_000011.8:g.47416106A>G	NCBI36
NG_008312.1:g.16201T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298854.7:c.1235T>C MANE Select	ENSP00000298854.2:p.Val412Ala
ENST00000298854.6:c.1235T>C	ENSP00000298854.2:p.Val412Ala
ENST00000352508.7:c.1058T>C	ENSP00000298853.3:p.Val353Ala
ENST00000524487.5:c.1076T>C	ENSP00000435551.2:p.Val359Ala
ENST00000528356.1:n.190T>C
NM_005055.4:c.1235T>C	NP_005046.2:p.Val412Ala
NM_032645.4:c.1058T>C	NP_116034.2:p.Val353Ala
XM_005253042.2:c.1181T>C	XP_005253099.1:p.Val394Ala
XM_005253043.2:c.1112T>C	XP_005253100.1:p.Val371Ala
XM_011520252.1:c.1320T>C	XP_011518554.1:p.Cys440=
XM_011520253.1:c.1259T>C	XP_011518555.1:p.Val420Ala
XM_005253042.3:c.1181T>C	XP_005253099.1:p.Val394Ala
XM_005253043.3:c.1112T>C	XP_005253100.1:p.Val371Ala
NM_005055.5:c.1235T>C MANE Select	NP_005046.2:p.Val412Ala
NM_032645.5:c.1058T>C	NP_116034.2:p.Val353Ala