Canonical Allele Identifier: CA397304485

Gene: C17orf107 CHRNE

Linked Data

• MyVariant Identifiers: chr17:g.4804146A>C (hg19) ; chr17:g.4900851A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4900851A>C , CM000679.2:g.4900851A>C	GRCh38
NC_000017.10:g.4804146A>C , CM000679.1:g.4804146A>C	GRCh37
NC_000017.9:g.4744925A>C	NCBI36
NG_008029.2:g.7225T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000381365.4:c.*318A>C (C17orf107) MANE Select	ENSP00000370770.3:n.*318A>C
ENST00000649488.2:c.859T>G (CHRNE) MANE Select	ENSP00000497829.1:p.Leu287Val
ENST00000649830.1:c.-75T>G (CHRNE)	ENSP00000496907.1:n.-75T>G
ENST00000293780.4:c.859T>G (CHRNE)	ENSP00000293780.4:p.Leu287Val
ENST00000381365.3:c.*318A>C (C17orf107)	ENSP00000370770.3:n.*318A>C
ENST00000572438.1:n.545T>G (CHRNE)
NM_000080.3:c.859T>G (CHRNE)	NP_000071.1:p.Leu287Val
NM_001145536.1:c.*318A>C (C17orf107)	NP_001139008.1:n.*318A>C
XM_011523612.1:c.546+345A>C (C17orf107)	XP_011521914.1:n.546+345A>C
XM_011523631.1:c.802+139T>G (CHRNE)	XP_011521933.1:n.802+139T>G
NM_000080.4:c.859T>G (CHRNE) MANE Select	NP_000071.1:p.Leu287Val
XM_017024115.1:c.823T>G (CHRNE)	XP_016879604.1:p.Leu275Val
XR_001752421.1:n.1647+139T>G (CHRNE)
NM_001145536.2:c.*318A>C (C17orf107) MANE Select	NP_001139008.1:n.*318A>C