Canonical Allele Identifier: CA387574912

Gene: RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24778357G>A , CM000675.2:g.24778357G>A	GRCh38
NC_000013.10:g.25352495G>A , CM000675.1:g.25352495G>A	GRCh37
NC_000013.9:g.24250495G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_031277.3:c.380G>A MANE Select	NP_112567.2:p.Arg127His
ENST00000255324.10:c.380G>A MANE Select	ENSP00000255324.5:p.Arg127His
NM_001184993.1:c.380G>A	NP_001171922.1:p.Arg127His
NM_001184993.2:c.380G>A	NP_001171922.1:p.Arg127His
NM_031277.2:c.380G>A	NP_112567.2:p.Arg127His
ENST00000255324.9:c.380G>A	ENSP00000255324.5:p.Arg127His
ENST00000255325.6:c.380G>A	ENSP00000255325.6:p.Arg127His
ENST00000255326.4:n.383G>A
XM_006719846.2:c.440G>A	XP_006719909.1:p.Arg147His
XM_006719846.3:c.440G>A	XP_006719909.1:p.Arg147His
XM_006719849.2:c.380G>A	XP_006719912.1:p.Arg127His
XM_006719852.2:c.-44G>A	XP_006719915.1:n.-44G>A
XM_011535152.1:c.461G>A	XP_011533454.1:p.Arg154His
XM_011535152.2:c.461G>A	XP_011533454.1:p.Arg154His
XM_011535153.1:c.461G>A	XP_011533455.1:p.Arg154His
XM_011535154.1:c.461G>A	XP_011533456.1:p.Arg154His
XM_011535155.1:c.461G>A	XP_011533457.1:p.Arg154His
XM_011535155.2:c.461G>A	XP_011533457.1:p.Arg154His
XM_011535156.1:c.461G>A	XP_011533458.1:p.Arg154His
XM_011535156.2:c.461G>A	XP_011533458.1:p.Arg154His
XM_011535157.1:c.461G>A	XP_011533459.1:p.Arg154His
XM_011535157.2:c.461G>A	XP_011533459.1:p.Arg154His
XM_011535158.1:c.461G>A	XP_011533460.1:p.Arg154His
XM_011535158.2:c.461G>A	XP_011533460.1:p.Arg154His
XM_011535159.1:c.461G>A	XP_011533461.1:p.Arg154His
XM_011535159.2:c.461G>A	XP_011533461.1:p.Arg154His
XM_011535160.1:c.461G>A	XP_011533462.1:p.Arg154His
XM_011535160.2:c.461G>A	XP_011533462.1:p.Arg154His
XM_011535161.1:c.287G>A	XP_011533463.1:p.Arg96His
XM_017020676.1:c.197G>A	XP_016876165.1:p.Arg66His