Canonical Allele Identifier: CA380337281

Gene: RAPSN

Linked Data

• gnomAD v4: 11-47448935-G-C
• MyVariant Identifiers: chr11:g.47470487G>C (hg19) ; chr11:g.47448935G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47448935G>C , CM000673.2:g.47448935G>C	GRCh38
NC_000011.9:g.47470487G>C , CM000673.1:g.47470487G>C	GRCh37
NC_000011.8:g.47427063G>C	NCBI36
NG_008312.1:g.5244C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298854.7:c.30C>G MANE Select	ENSP00000298854.2:p.Ile10Met
ENST00000298854.6:c.30C>G	ENSP00000298854.2:p.Ile10Met
ENST00000352508.7:c.30C>G	ENSP00000298853.3:p.Ile10Met
ENST00000524487.5:c.30C>G	ENSP00000435551.2:p.Ile10Met
ENST00000529341.1:c.30C>G	ENSP00000431732.1:p.Ile10Met
NM_005055.4:c.30C>G	NP_005046.2:p.Ile10Met
NM_032645.4:c.30C>G	NP_116034.2:p.Ile10Met
XM_005253042.2:c.30C>G	XP_005253099.1:p.Ile10Met
XM_005253043.2:c.30C>G	XP_005253100.1:p.Ile10Met
XM_011520252.1:c.30C>G	XP_011518554.1:p.Ile10Met
XM_011520253.1:c.30C>G	XP_011518555.1:p.Ile10Met
XM_005253042.3:c.30C>G	XP_005253099.1:p.Ile10Met
XM_005253043.3:c.30C>G	XP_005253100.1:p.Ile10Met
NM_005055.5:c.30C>G MANE Select	NP_005046.2:p.Ile10Met
NM_032645.5:c.30C>G	NP_116034.2:p.Ile10Met