Canonical Allele Identifier: CA1742553

Gene: RNF181

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85595797C>A , CM000664.2:g.85595797C>A	GRCh38
NC_000002.11:g.85822920C>A , CM000664.1:g.85822920C>A	GRCh37
NC_000002.10:g.85676431C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016494.4:c.34C>A MANE Select	NP_057578.1:p.Pro12Thr
ENST00000306368.9:c.34C>A MANE Select	ENSP00000306906.4:p.Pro12Thr
NM_016494.3:c.34C>A	NP_057578.1:p.Pro12Thr
ENST00000306368.8:c.34C>A	ENSP00000306906.4:p.Pro12Thr
ENST00000414390.5:c.34C>A	ENSP00000397109.1:p.Pro12Thr
ENST00000441634.5:c.34C>A	ENSP00000412025.1:p.Pro12Thr
ENST00000443647.5:c.34C>A	ENSP00000391326.1:p.Pro12Thr
ENST00000461845.1:n.73C>A
XM_005264359.3:c.34C>A	XP_005264416.1:p.Pro12Thr
XM_005264359.4:c.34C>A	XP_005264416.1:p.Pro12Thr