Canonical Allele Identifier: CA2808296152

Gene: CHRNE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4898632_4898633insA , CM000679.2:g.4898632_4898633insA	GRCh38
NC_000017.10:g.4801927_4801928insA , CM000679.1:g.4801927_4801928insA	GRCh37
NC_000017.9:g.4742706_4742707insA	NCBI36
NG_008029.2:g.9443_9444insT
NG_028005.1:g.70293_70294insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649488.2:c.*103_*104insT MANE Select	ENSP00000497829.1:n.*103_*104insT
ENST00000649830.1:c.*221_*222insT	ENSP00000496907.1:n.*221_*222insT
ENST00000652550.1:n.1311_1312insT
ENST00000293780.4:c.*103_*104insT	ENSP00000293780.4:n.*103_*104insT
ENST00000572438.1:n.1271_1272insT
NM_000080.3:c.*103_*104insT	NP_000071.1:n.*103_*104insT
NM_000080.4:c.*103_*104insT MANE Select	NP_000071.1:n.*103_*104insT
XM_017024115.1:c.*103_*104insT	XP_016879604.1:n.*103_*104insT