Canonical Allele Identifier: CA397304471

Gene: C17orf107 CHRNE

Linked Data

• MyVariant Identifiers: chr17:g.4804142A>T (hg19) ; chr17:g.4900847A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4900847A>T , CM000679.2:g.4900847A>T	GRCh38
NC_000017.10:g.4804142A>T , CM000679.1:g.4804142A>T	GRCh37
NC_000017.9:g.4744921A>T	NCBI36
NG_008029.2:g.7229T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381365.4:c.*314A>T (C17orf107) MANE Select	ENSP00000370770.3:n.*314A>T
ENST00000649488.2:c.863T>A (CHRNE) MANE Select	ENSP00000497829.1:p.Phe288Tyr
ENST00000649830.1:c.-71T>A (CHRNE)	ENSP00000496907.1:n.-71T>A
ENST00000293780.4:c.863T>A (CHRNE)	ENSP00000293780.4:p.Phe288Tyr
ENST00000381365.3:c.*314A>T (C17orf107)	ENSP00000370770.3:n.*314A>T
ENST00000572438.1:n.549T>A (CHRNE)
NM_000080.3:c.863T>A (CHRNE)	NP_000071.1:p.Phe288Tyr
NM_001145536.1:c.*314A>T (C17orf107)	NP_001139008.1:n.*314A>T
XM_011523612.1:c.546+341A>T (C17orf107)	XP_011521914.1:n.546+341A>T
XM_011523631.1:c.802+143T>A (CHRNE)	XP_011521933.1:n.802+143T>A
NM_000080.4:c.863T>A (CHRNE) MANE Select	NP_000071.1:p.Phe288Tyr
XM_017024115.1:c.827T>A (CHRNE)	XP_016879604.1:p.Phe276Tyr
XR_001752421.1:n.1647+143T>A (CHRNE)
NM_001145536.2:c.*314A>T (C17orf107) MANE Select	NP_001139008.1:n.*314A>T