Canonical Allele Identifier: CA624856071

Gene: C17orf107 CHRNE

Linked Data

• dbSNP Id: rs1156609634
• gnomAD v2: 17-4805500-C-A
• gnomAD v4: 17-4902205-C-A
• MyVariant Identifiers: chr17:g.4805500C>A (hg19) ; chr17:g.4902205C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4902205C>A , CM000679.2:g.4902205C>A	GRCh38
NC_000017.10:g.4805500C>A , CM000679.1:g.4805500C>A	GRCh37
NC_000017.9:g.4746279C>A	NCBI36
NG_008029.2:g.5871G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381365.4:c.*1672C>A (C17orf107) MANE Select	ENSP00000370770.3:n.*1672C>A
ENST00000649488.2:c.344+12G>T (CHRNE) MANE Select	ENSP00000497829.1:n.344+12G>T
ENST00000649830.1:c.-590+12G>T (CHRNE)	ENSP00000496907.1:n.-590+12G>T
ENST00000293780.4:c.344+12G>T (CHRNE)	ENSP00000293780.4:n.344+12G>T
ENST00000381365.3:c.*1672C>A (C17orf107)	ENSP00000370770.3:n.*1672C>A
ENST00000575637.1:n.165+12G>T (CHRNE)
NM_000080.3:c.344+12G>T (CHRNE)	NP_000071.1:n.344+12G>T
NM_001145536.1:c.*1672C>A (C17orf107)	NP_001139008.1:n.*1672C>A
XM_011523612.1:c.546+1699C>A (C17orf107)	XP_011521914.1:n.546+1699C>A
XM_011523631.1:c.344+12G>T (CHRNE)	XP_011521933.1:n.344+12G>T
NM_000080.4:c.344+12G>T (CHRNE) MANE Select	NP_000071.1:n.344+12G>T
XM_017024115.1:c.308+12G>T (CHRNE)	XP_016879604.1:n.308+12G>T
XR_001752421.1:n.1189+12G>T (CHRNE)
NM_001145536.2:c.*1672C>A (C17orf107) MANE Select	NP_001139008.1:n.*1672C>A