Canonical Allele Identifier: CA497677040

Gene: C17orf107 CHRNE

Linked Data

• gnomAD v4: 17-4902273-T-C
• MyVariant Identifiers: chr17:g.4805568T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4902273T>C , CM000679.2:g.4902273T>C	GRCh38
NC_000017.10:g.4805568T>C , CM000679.1:g.4805568T>C	GRCh37
NC_000017.9:g.4746347T>C	NCBI36
NG_008029.2:g.5803A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000381365.4:c.*1740T>C (C17orf107) MANE Select	ENSP00000370770.3:n.*1740T>C
ENST00000649488.2:c.288A>G (CHRNE) MANE Select	ENSP00000497829.1:p.Glu96=
ENST00000649830.1:c.-646A>G (CHRNE)	ENSP00000496907.1:n.-646A>G
ENST00000293780.4:c.288A>G (CHRNE)	ENSP00000293780.4:p.Glu96=
ENST00000381365.3:c.*1740T>C (C17orf107)	ENSP00000370770.3:n.*1740T>C
ENST00000575637.1:n.109A>G (CHRNE)
NM_000080.3:c.288A>G (CHRNE)	NP_000071.1:p.Glu96=
NM_001145536.1:c.*1740T>C (C17orf107)	NP_001139008.1:n.*1740T>C
XM_011523612.1:c.546+1767T>C (C17orf107)	XP_011521914.1:n.546+1767T>C
XM_011523631.1:c.288A>G (CHRNE)	XP_011521933.1:p.Glu96=
NM_000080.4:c.288A>G (CHRNE) MANE Select	NP_000071.1:p.Glu96=
XM_017024115.1:c.252A>G (CHRNE)	XP_016879604.1:p.Glu84=
XR_001752421.1:n.1133A>G (CHRNE)
NM_001145536.2:c.*1740T>C (C17orf107) MANE Select	NP_001139008.1:n.*1740T>C