Canonical Allele Identifier: CA2635577250

Gene: CHRNE

Linked Data

• gnomAD v4: 17-4898637-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898637C>A , CM000679.2:g.4898637C>A	GRCh38
NC_000017.10:g.4801932C>A , CM000679.1:g.4801932C>A	GRCh37
NC_000017.9:g.4742711C>A	NCBI36
NG_008029.2:g.9439G>T
NG_028005.1:g.70298C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.*99G>T MANE Select	ENSP00000497829.1:n.*99G>T
ENST00000649830.1:c.*217G>T	ENSP00000496907.1:n.*217G>T
ENST00000652550.1:n.1307G>T
ENST00000293780.4:c.*99G>T	ENSP00000293780.4:n.*99G>T
ENST00000572438.1:n.1267G>T
NM_000080.3:c.*99G>T	NP_000071.1:n.*99G>T
NM_000080.4:c.*99G>T MANE Select	NP_000071.1:n.*99G>T
XM_017024115.1:c.*99G>T	XP_016879604.1:n.*99G>T