Canonical Allele Identifier: CA2244609850
Gene: CHRNE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4898088_4898089delinsTC , CM000679.2:g.4898088_4898089delinsTC GRCh38
NC_000017.10:g.4801383_4801384delinsTC , CM000679.1:g.4801383_4801384delinsTC GRCh37
NC_000017.9:g.4742162_4742163delinsTC NCBI36
NG_008029.2:g.9987_9988delinsGA
NG_028005.1:g.69749_69750delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000649488.2:c.*647_*648delinsGA MANE Select ENSP00000497829.1:n.*647_*648delinsGA
ENST00000649830.1:c.*765_*766delinsGA ENSP00000496907.1:n.*765_*766delinsGA
ENST00000652550.1:n.1855_1856delinsGA
ENST00000293780.4:c.*647_*648delinsGA ENSP00000293780.4:n.*647_*648delinsGA
ENST00000572438.1:n.1815_1816delinsGA
NM_000080.3:c.*647_*648delinsGA NP_000071.1:n.*647_*648delinsGA
NM_000080.4:c.*647_*648delinsGA MANE Select NP_000071.1:n.*647_*648delinsGA
XM_017024115.1:c.*647_*648delinsGA XP_016879604.1:n.*647_*648delinsGA