Canonical Allele Identifier: CA497676562

Gene: C17orf107 CHRNE

Linked Data

• gnomAD v4: 17-4900849-C-T
• MyVariant Identifiers: chr17:g.4804144C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4900849C>T , CM000679.2:g.4900849C>T	GRCh38
NC_000017.10:g.4804144C>T , CM000679.1:g.4804144C>T	GRCh37
NC_000017.9:g.4744923C>T	NCBI36
NG_008029.2:g.7227G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381365.4:c.*316C>T (C17orf107) MANE Select	ENSP00000370770.3:n.*316C>T
ENST00000649488.2:c.861G>A (CHRNE) MANE Select	ENSP00000497829.1:p.Leu287=
ENST00000649830.1:c.-73G>A (CHRNE)	ENSP00000496907.1:n.-73G>A
ENST00000293780.4:c.861G>A (CHRNE)	ENSP00000293780.4:p.Leu287=
ENST00000381365.3:c.*316C>T (C17orf107)	ENSP00000370770.3:n.*316C>T
ENST00000572438.1:n.547G>A (CHRNE)
NM_000080.3:c.861G>A (CHRNE)	NP_000071.1:p.Leu287=
NM_001145536.1:c.*316C>T (C17orf107)	NP_001139008.1:n.*316C>T
XM_011523612.1:c.546+343C>T (C17orf107)	XP_011521914.1:n.546+343C>T
XM_011523631.1:c.802+141G>A (CHRNE)	XP_011521933.1:n.802+141G>A
NM_000080.4:c.861G>A (CHRNE) MANE Select	NP_000071.1:p.Leu287=
XM_017024115.1:c.825G>A (CHRNE)	XP_016879604.1:p.Leu275=
XR_001752421.1:n.1647+141G>A (CHRNE)
NM_001145536.2:c.*316C>T (C17orf107) MANE Select	NP_001139008.1:n.*316C>T