Canonical Allele Identifier: CA387578562

Gene: RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24793276T>G , CM000675.2:g.24793276T>G	GRCh38
NC_000013.10:g.25367414T>G , CM000675.1:g.25367414T>G	GRCh37
NC_000013.9:g.24265414T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255324.10:c.1170T>G MANE Select	ENSP00000255324.5:p.Ile390Met
ENST00000255324.9:c.1170T>G	ENSP00000255324.5:p.Ile390Met
ENST00000255325.6:c.1170T>G	ENSP00000255325.6:p.Ile390Met
ENST00000255326.4:n.1173T>G
NM_001184993.1:c.1170T>G	NP_001171922.1:p.Ile390Met
NM_031277.2:c.1170T>G	NP_112567.2:p.Ile390Met
XM_006719846.2:c.1230T>G	XP_006719909.1:p.Ile410Met
XM_006719849.2:c.1170T>G	XP_006719912.1:p.Ile390Met
XM_006719852.2:c.747T>G	XP_006719915.1:p.Ile249Met
XM_011535152.1:c.1251T>G	XP_011533454.1:p.Ile417Met
XM_011535153.1:c.1251T>G	XP_011533455.1:p.Ile417Met
XM_011535154.1:c.1251T>G	XP_011533456.1:p.Ile417Met
XM_011535155.1:c.1251T>G	XP_011533457.1:p.Ile417Met
XM_011535156.1:c.1251T>G	XP_011533458.1:p.Ile417Met
XM_011535157.1:c.1251T>G	XP_011533459.1:p.Ile417Met
XM_011535158.1:c.1251T>G	XP_011533460.1:p.Ile417Met
XM_011535159.1:c.1251T>G	XP_011533461.1:p.Ile417Met
XM_011535160.1:c.1251T>G	XP_011533462.1:p.Ile417Met
XM_011535161.1:c.1077T>G	XP_011533463.1:p.Ile359Met
XM_011535162.1:c.648T>G	XP_011533464.1:p.Ile216Met
XM_006719846.3:c.1230T>G	XP_006719909.1:p.Ile410Met
XM_011535152.2:c.1251T>G	XP_011533454.1:p.Ile417Met
XM_011535155.2:c.1251T>G	XP_011533457.1:p.Ile417Met
XM_011535156.2:c.1251T>G	XP_011533458.1:p.Ile417Met
XM_011535157.2:c.1251T>G	XP_011533459.1:p.Ile417Met
XM_011535158.2:c.1251T>G	XP_011533460.1:p.Ile417Met
XM_011535159.2:c.1251T>G	XP_011533461.1:p.Ile417Met
XM_011535160.2:c.1251T>G	XP_011533462.1:p.Ile417Met
XM_017020676.1:c.987T>G	XP_016876165.1:p.Ile329Met
NM_031277.3:c.1170T>G MANE Select	NP_112567.2:p.Ile390Met
NM_001184993.2:c.1170T>G	NP_001171922.1:p.Ile390Met