Canonical Allele Identifier: CA2830535145

Gene: RNF175

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153728373_153728374insGATACTTCCTGTTCATTTCTCTGACAGCTGG , CM000666.2:g.153728373_153728374insGATACTTCCTGTTCATTTCTCTGACAGCTGG	GRCh38
NC_000004.11:g.154649525_154649526insGATACTTCCTGTTCATTTCTCTGACAGCTGG , CM000666.1:g.154649525_154649526insGATACTTCCTGTTCATTTCTCTGACAGCTGG	GRCh37
NC_000004.10:g.154868975_154868976insGATACTTCCTGTTCATTTCTCTGACAGCTGG	NCBI36
NG_016386.1:g.36862_36863insCCAGCTGTCAGAGAAATGAACAGGAAGTATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347063.9:c.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC MANE Select	ENSP00000340979.4:n.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGA...
ENST00000347063.8:c.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	ENSP00000340979.4:n.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGA...
ENST00000503694.5:c.247-4916_247-4915insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	ENSP00000424430.1:n.247-4916_247-4915insCCAGCTGTCAGAGAAATGAAC...
ENST00000506505.1:n.382-4916_382-4915insCCAGCTGTCAGAGAAATGAACAGGAAGTATC
ENST00000507512.1:c.*81-13_*81-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	ENSP00000424563.1:n.*81-13_*81-12insCCAGCTGTCAGAGAAATGAACAGGA...
ENST00000508248.1:c.67-13_67-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	ENSP00000427472.1:n.67-13_67-12insCCAGCTGTCAGAGAAATGAACAGGAAG...
ENST00000508967.5:n.165-13_165-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC
ENST00000513656.5:c.105-13_105-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	ENSP00000421761.1:n.105-13_105-12insCCAGCTGTCAGAGAAATGAACAGGA...
NM_173662.2:c.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	NP_775933.1:n.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC...
XM_005262938.2:c.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_005262995.1:n.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGT...
XM_005262939.2:c.7-13_7-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_005262996.1:n.7-13_7-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC
XM_005262940.3:c.4-13_4-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_005262997.1:n.4-13_4-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC
XM_011531879.1:c.306-4916_306-4915insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530181.1:n.306-4916_306-4915insCCAGCTGTCAGAGAAATGAACAGG...
XM_011531880.1:c.127-13_127-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530182.1:n.127-13_127-12insCCAGCTGTCAGAGAAATGAACAGGAAGT...
XM_011531881.1:c.127-13_127-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530183.1:n.127-13_127-12insCCAGCTGTCAGAGAAATGAACAGGAAGT...
XM_011531882.1:c.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530184.1:n.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGT...
XM_011531883.1:c.186-4916_186-4915insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530185.1:n.186-4916_186-4915insCCAGCTGTCAGAGAAATGAACAGG...
XM_011531884.1:c.-18-13_-18-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530186.1:n.-18-13_-18-12insCCAGCTGTCAGAGAAATGAACAGGAAGT...
XM_011531885.1:c.7-13_7-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530187.1:n.7-13_7-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC
XR_939365.1:n.401+5079_401+5080insGATACTTCCTGTTCATTTCTCTGACAGCTGG
XR_939366.1:n.309+5079_309+5080insGATACTTCCTGTTCATTTCTCTGACAGCTGG
XM_005262938.3:c.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_005262995.1:n.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGT...
XM_005262939.3:c.7-13_7-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_005262996.1:n.7-13_7-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC
XM_005262940.4:c.4-13_4-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_005262997.1:n.4-13_4-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC
XM_011531879.2:c.306-4916_306-4915insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530181.1:n.306-4916_306-4915insCCAGCTGTCAGAGAAATGAACAGG...
XM_011531881.2:c.127-13_127-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530183.1:n.127-13_127-12insCCAGCTGTCAGAGAAATGAACAGGAAGT...
XM_011531882.2:c.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530184.1:n.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGT...
XM_011531883.2:c.186-4916_186-4915insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_011530185.1:n.186-4916_186-4915insCCAGCTGTCAGAGAAATGAACAGG...
XM_017008047.1:c.105-4916_105-4915insCCAGCTGTCAGAGAAATGAACAGGAAGTATC	XP_016863536.1:n.105-4916_105-4915insCCAGCTGTCAGAGAAATGAACAGG...
XR_001741890.1:n.2086+5079_2086+5080insGATACTTCCTGTTCATTTCTCTGACAGCTGG
XR_001741891.1:n.2286+5079_2286+5080insGATACTTCCTGTTCATTTCTCTGACAGCTGG
NM_173662.4:c.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC MANE Select	NP_775933.2:n.247-13_247-12insCCAGCTGTCAGAGAAATGAACAGGAAGTATC...