Canonical Allele Identifier: CA2635577248

Gene: CHRNE

Linked Data

• gnomAD v4: 17-4898636-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898636T>A , CM000679.2:g.4898636T>A	GRCh38
NC_000017.10:g.4801931T>A , CM000679.1:g.4801931T>A	GRCh37
NC_000017.9:g.4742710T>A	NCBI36
NG_008029.2:g.9440A>T
NG_028005.1:g.70297T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.*100A>T MANE Select	ENSP00000497829.1:n.*100A>T
ENST00000649830.1:c.*218A>T	ENSP00000496907.1:n.*218A>T
ENST00000652550.1:n.1308A>T
ENST00000293780.4:c.*100A>T	ENSP00000293780.4:n.*100A>T
ENST00000572438.1:n.1268A>T
NM_000080.3:c.*100A>T	NP_000071.1:n.*100A>T
NM_000080.4:c.*100A>T MANE Select	NP_000071.1:n.*100A>T
XM_017024115.1:c.*100A>T	XP_016879604.1:n.*100A>T