Canonical Allele Identifier: CA474220535

Gene: RAPSN

Linked Data

• dbSNP Id: rs770689515
• gnomAD v4: 11-47448926-C-G
• MyVariant Identifiers: chr11:g.47470478C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47448926C>G , CM000673.2:g.47448926C>G	GRCh38
NC_000011.9:g.47470478C>G , CM000673.1:g.47470478C>G	GRCh37
NC_000011.8:g.47427054C>G	NCBI36
NG_008312.1:g.5253G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298854.7:c.39G>C MANE Select	ENSP00000298854.2:p.Gly13=
ENST00000298854.6:c.39G>C	ENSP00000298854.2:p.Gly13=
ENST00000352508.7:c.39G>C	ENSP00000298853.3:p.Gly13=
ENST00000524487.5:c.39G>C	ENSP00000435551.2:p.Gly13=
ENST00000529341.1:c.39G>C	ENSP00000431732.1:p.Gly13=
NM_005055.4:c.39G>C	NP_005046.2:p.Gly13=
NM_032645.4:c.39G>C	NP_116034.2:p.Gly13=
XM_005253042.2:c.39G>C	XP_005253099.1:p.Gly13=
XM_005253043.2:c.39G>C	XP_005253100.1:p.Gly13=
XM_011520252.1:c.39G>C	XP_011518554.1:p.Gly13=
XM_011520253.1:c.39G>C	XP_011518555.1:p.Gly13=
XM_005253042.3:c.39G>C	XP_005253099.1:p.Gly13=
XM_005253043.3:c.39G>C	XP_005253100.1:p.Gly13=
NM_005055.5:c.39G>C MANE Select	NP_005046.2:p.Gly13=
NM_032645.5:c.39G>C	NP_116034.2:p.Gly13=