Canonical Allele Identifier: CA2244612748

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4902279_4902280delinsAC , CM000679.2:g.4902279_4902280delinsAC	GRCh38
NC_000017.10:g.4805574_4805575delinsAC , CM000679.1:g.4805574_4805575delinsAC	GRCh37
NC_000017.9:g.4746353_4746354delinsAC	NCBI36
NG_008029.2:g.5796_5797delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000381365.4:c.*1746_*1747delinsAC (C17orf107) MANE Select	ENSP00000370770.3:n.*1746_*1747delinsAC
ENST00000649488.2:c.281_282delinsGT (CHRNE) MANE Select	ENSP00000497829.1:p.Gly94=
ENST00000649830.1:c.-653_-652delinsGT (CHRNE)	ENSP00000496907.1:n.-653_-652delinsGT
ENST00000293780.4:c.281_282delinsGT (CHRNE)	ENSP00000293780.4:p.Gly94=
ENST00000381365.3:c.*1746_*1747delinsAC (C17orf107)	ENSP00000370770.3:n.*1746_*1747delinsAC
ENST00000575637.1:n.102_103delinsGT (CHRNE)
NM_000080.3:c.281_282delinsGT (CHRNE)	NP_000071.1:p.Gly94=
NM_001145536.1:c.*1746_*1747delinsAC (C17orf107)	NP_001139008.1:n.*1746_*1747delinsAC
XM_011523612.1:c.546+1773_546+1774delinsAC (C17orf107)	XP_011521914.1:n.546+1773_546+1774delinsA...
XM_011523631.1:c.281_282delinsGT (CHRNE)	XP_011521933.1:p.Gly94=
NM_000080.4:c.281_282delinsGT (CHRNE) MANE Select	NP_000071.1:p.Gly94=
XM_017024115.1:c.245_246delinsGT (CHRNE)	XP_016879604.1:p.Gly82=
XR_001752421.1:n.1126_1127delinsGT (CHRNE)
NM_001145536.2:c.*1746_*1747delinsAC (C17orf107) MANE Select	NP_001139008.1:n.*1746_*1747delinsAC