Canonical Allele Identifier: CA1844678999

Gene: RIGI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32523755_32523756delinsAC , CM000671.2:g.32523755_32523756delinsAC	GRCh38
NC_000009.11:g.32523753_32523754delinsAC , CM000671.1:g.32523753_32523754delinsAC	GRCh37
NC_000009.10:g.32513753_32513754delinsAC	NCBI36
NG_046918.1:g.7569_7570delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000379868.6:c.106+2305_106+2306delinsGT	ENSP00000369197.2:n.106+2305_106+2306deli...
ENST00000379883.3:c.106+2305_106+2306delinsGT MANE Select	ENSP00000369213.2:n.106+2305_106+2306deli...
ENST00000679662.1:n.104+2305_104+2306delinsGT
ENST00000679771.1:c.106+2305_106+2306delinsGT	ENSP00000505015.1:n.106+2305_106+2306deli...
ENST00000679859.1:c.106+2305_106+2306delinsGT	ENSP00000505702.1:n.106+2305_106+2306deli...
ENST00000680198.1:c.199-22820_199-22819delinsGT	ENSP00000505143.1:n.199-22820_199-22819de...
ENST00000680733.1:c.110+2301_110+2302delinsGT	ENSP00000504892.1:n.110+2301_110+2302deli...
ENST00000680883.1:n.104+2305_104+2306delinsGT
ENST00000681750.1:c.-44-22817_-44-22816delinsGT	ENSP00000506413.1:n.-44-22817_-44-22816de...
ENST00000379868.5:c.-356+2305_-356+2306delinsGT	ENSP00000369197.1:n.-356+2305_-356+2306de...
ENST00000379883.2:c.106+2305_106+2306delinsGT	ENSP00000369213.2:n.106+2305_106+2306deli...
NM_014314.3:c.106+2305_106+2306delinsGT	NP_055129.2:n.106+2305_106+2306delinsGT
NM_014314.4:c.106+2305_106+2306delinsGT MANE Select	NP_055129.2:n.106+2305_106+2306delinsGT
NM_001385907.1:c.106+2305_106+2306delinsGT	NP_001372836.1:n.106+2305_106+2306delinsG...
NM_001385909.1:c.106+2305_106+2306delinsGT	NP_001372838.1:n.106+2305_106+2306delinsG...
NM_001385910.1:c.-349+2305_-349+2306delinsGT	NP_001372839.1:n.-349+2305_-349+2306delin...
NM_001385912.1:c.-356+2305_-356+2306delinsGT	NP_001372841.1:n.-356+2305_-356+2306delin...
NM_001385913.1:c.106+2305_106+2306delinsGT	NP_001372842.1:n.106+2305_106+2306delinsG...
NM_001385914.1:c.-349+2305_-349+2306delinsGT	NP_001372843.1:n.-349+2305_-349+2306delin...