Canonical Allele Identifier: CA387583368

Gene: RNF17

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.24804316T>C , CM000675.2:g.24804316T>C	GRCh38
NC_000013.10:g.25378454T>C , CM000675.1:g.25378454T>C	GRCh37
NC_000013.9:g.24276454T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_031277.3:c.1978T>C MANE Select	NP_112567.2:p.Phe660Leu
ENST00000255324.10:c.1978T>C MANE Select	ENSP00000255324.5:p.Phe660Leu
NM_001184993.1:c.1978T>C	NP_001171922.1:p.Phe660Leu
NM_001184993.2:c.1978T>C	NP_001171922.1:p.Phe660Leu
NM_031277.2:c.1978T>C	NP_112567.2:p.Phe660Leu
ENST00000255324.9:c.1978T>C	ENSP00000255324.5:p.Phe660Leu
ENST00000255325.6:c.1949+1745T>C	ENSP00000255325.6:n.1949+1745T>C
ENST00000418120.5:c.-51T>C	ENSP00000388892.1:n.-51T>C
XM_006719846.2:c.2038T>C	XP_006719909.1:p.Phe680Leu
XM_006719846.3:c.2038T>C	XP_006719909.1:p.Phe680Leu
XM_006719849.2:c.1978T>C	XP_006719912.1:p.Phe660Leu
XM_006719852.2:c.1555T>C	XP_006719915.1:p.Phe519Leu
XM_011535152.1:c.2059T>C	XP_011533454.1:p.Phe687Leu
XM_011535152.2:c.2059T>C	XP_011533454.1:p.Phe687Leu
XM_011535153.1:c.2059T>C	XP_011533455.1:p.Phe687Leu
XM_011535154.1:c.2059T>C	XP_011533456.1:p.Phe687Leu
XM_011535155.1:c.2059T>C	XP_011533457.1:p.Phe687Leu
XM_011535155.2:c.2059T>C	XP_011533457.1:p.Phe687Leu
XM_011535156.1:c.2059T>C	XP_011533458.1:p.Phe687Leu
XM_011535156.2:c.2059T>C	XP_011533458.1:p.Phe687Leu
XM_011535157.1:c.2059T>C	XP_011533459.1:p.Phe687Leu
XM_011535157.2:c.2059T>C	XP_011533459.1:p.Phe687Leu
XM_011535158.1:c.2059T>C	XP_011533460.1:p.Phe687Leu
XM_011535158.2:c.2059T>C	XP_011533460.1:p.Phe687Leu
XM_011535159.1:c.2059T>C	XP_011533461.1:p.Phe687Leu
XM_011535159.2:c.2059T>C	XP_011533461.1:p.Phe687Leu
XM_011535160.1:c.2059T>C	XP_011533462.1:p.Phe687Leu
XM_011535160.2:c.2059T>C	XP_011533462.1:p.Phe687Leu
XM_011535161.1:c.1885T>C	XP_011533463.1:p.Phe629Leu
XM_011535162.1:c.1456T>C	XP_011533464.1:p.Phe486Leu
XM_011535163.1:c.745T>C	XP_011533465.1:p.Phe249Leu
XM_017020676.1:c.1795T>C	XP_016876165.1:p.Phe599Leu