Canonical Allele Identifier: CA2244609869
Gene: CHRNE HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898111A= , CM000679.2:g.4898111A= GRCh38
NC_000017.10:g.4801406A= , CM000679.1:g.4801406A= GRCh37
NC_000017.9:g.4742185A= NCBI36
NG_008029.2:g.9965T=
NG_028005.1:g.69772A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*625T= MANE Select ENSP00000497829.1:n.*625T=
ENST00000649830.1:c.*743T= ENSP00000496907.1:n.*743T=
ENST00000652550.1:n.1833T=
ENST00000293780.4:c.*625T= ENSP00000293780.4:n.*625T=
ENST00000572438.1:n.1793T=
NM_000080.3:c.*625T= NP_000071.1:n.*625T=
NM_000080.4:c.*625T= MANE Select NP_000071.1:n.*625T=
XM_017024115.1:c.*625T= XP_016879604.1:n.*625T=
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