Canonical Allele Identifier: CA2733114392

Gene: C17orf107 CHRNE

Linked Data

• dbSNP Id: rs2151096933

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4900746C>G , CM000679.2:g.4900746C>G	GRCh38
NC_000017.10:g.4804041C>G , CM000679.1:g.4804041C>G	GRCh37
NC_000017.9:g.4744820C>G	NCBI36
NG_008029.2:g.7330G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381365.4:c.*213C>G (C17orf107) MANE Select	ENSP00000370770.3:n.*213C>G
ENST00000649488.2:c.917+47G>C (CHRNE) MANE Select	ENSP00000497829.1:n.917+47G>C
ENST00000649830.1:c.-17+47G>C (CHRNE)	ENSP00000496907.1:n.-17+47G>C
ENST00000293780.4:c.917+47G>C (CHRNE)	ENSP00000293780.4:n.917+47G>C
ENST00000381365.3:c.*213C>G (C17orf107)	ENSP00000370770.3:n.*213C>G
ENST00000521575.1:c.*580C>G (C17orf107)	ENSP00000429241.1:n.*580C>G
ENST00000572438.1:n.603+47G>C (CHRNE)
NM_000080.3:c.917+47G>C (CHRNE)	NP_000071.1:n.917+47G>C
NM_001145536.1:c.*213C>G (C17orf107)	NP_001139008.1:n.*213C>G
XM_011523612.1:c.546+240C>G (C17orf107)	XP_011521914.1:n.546+240C>G
XM_011523631.1:c.802+244G>C (CHRNE)	XP_011521933.1:n.802+244G>C
NM_000080.4:c.917+47G>C (CHRNE) MANE Select	NP_000071.1:n.917+47G>C
XM_017024115.1:c.881+47G>C (CHRNE)	XP_016879604.1:n.881+47G>C
XR_001752421.1:n.1647+244G>C (CHRNE)
NM_001145536.2:c.*213C>G (C17orf107) MANE Select	NP_001139008.1:n.*213C>G