Canonical Allele Identifier: CA2695201220

Gene: CHRNE C17orf107

Linked Data

• ClinVar Variation Id: 2680785
• ClinVar RCV Id: RCV003468425

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4899514_4899516delinsA , CM000679.2:g.4899514_4899516delinsA	GRCh38
NC_000017.10:g.4802809_4802811delinsA , CM000679.1:g.4802809_4802811delinsA	GRCh37
NC_000017.9:g.4743588_4743590delinsA	NCBI36
NG_008029.2:g.8560_8562delinsT
NG_028005.1:g.71175_71177delinsA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.984_986delinsT (CHRNE) MANE Select	ENSP00000497829.1:p.Ser329ProfsTer?
ENST00000649830.1:c.51_53delinsT (CHRNE)	ENSP00000496907.1:p.Ser18ProfsTer?
ENST00000652550.1:n.714_716delinsT (CHRNE)
ENST00000293780.4:c.984_986delinsT (CHRNE)	ENSP00000293780.4:p.Ser329ProfsTer?
ENST00000521575.1:c.-249_-247delinsA (C17orf107)	ENSP00000429241.1:n.-249_-247delinsA
ENST00000572438.1:n.670_672delinsT (CHRNE)
NM_000080.3:c.984_986delinsT (CHRNE)	NP_000071.1:p.Ser329ProfsTer?
XM_011523612.1:c.-249_-247delinsA (C17orf107)	XP_011521914.1:n.-249_-247delinsA
XM_011523631.1:c.*23_*25delinsT (CHRNE)	XP_011521933.1:n.*23_*25delinsT
NM_000080.4:c.984_986delinsT (CHRNE) MANE Select	NP_000071.1:p.Ser329ProfsTer?
XM_017024115.1:c.948_950delinsT (CHRNE)	XP_016879604.1:p.Ser317ProfsTer?
XR_001752421.1:n.1714_1716delinsT (CHRNE)