Canonical Allele Identifier: CA2244611798

Gene: C17orf107 CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4900853_4900855delinsAAG , CM000679.2:g.4900853_4900855delinsAAG	GRCh38
NC_000017.10:g.4804148_4804150delinsAAG , CM000679.1:g.4804148_4804150delinsAAG	GRCh37
NC_000017.9:g.4744927_4744929delinsAAG	NCBI36
NG_008029.2:g.7221_7223delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000381365.4:c.*320_*322delinsAAG (C17orf107) MANE Select	ENSP00000370770.3:n.*320_*322delinsAAG
ENST00000649488.2:c.855_857delinsCTT (CHRNE) MANE Select	ENSP00000497829.1:p.Val285=
ENST00000649830.1:c.-79_-77delinsCTT (CHRNE)	ENSP00000496907.1:n.-79_-77delinsCTT
ENST00000293780.4:c.855_857delinsCTT (CHRNE)	ENSP00000293780.4:p.Val285=
ENST00000381365.3:c.*320_*322delinsAAG (C17orf107)	ENSP00000370770.3:n.*320_*322delinsAAG
ENST00000572438.1:n.541_543delinsCTT (CHRNE)
NM_000080.3:c.855_857delinsCTT (CHRNE)	NP_000071.1:p.Val285=
NM_001145536.1:c.*320_*322delinsAAG (C17orf107)	NP_001139008.1:n.*320_*322delinsAAG
XM_011523612.1:c.546+347_546+349delinsAAG (C17orf107)	XP_011521914.1:n.546+347_546+349delinsAAG...
XM_011523631.1:c.802+135_802+137delinsCTT (CHRNE)	XP_011521933.1:n.802+135_802+137delinsCTT...
NM_000080.4:c.855_857delinsCTT (CHRNE) MANE Select	NP_000071.1:p.Val285=
XM_017024115.1:c.819_821delinsCTT (CHRNE)	XP_016879604.1:p.Val273=
XR_001752421.1:n.1647+135_1647+137delinsCTT (CHRNE)
NM_001145536.2:c.*320_*322delinsAAG (C17orf107) MANE Select	NP_001139008.1:n.*320_*322delinsAAG