Canonical Allele Identifier: CA2653785164

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350906-GGAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350911_63350913del , CM000682.2:g.63350911_63350913del	GRCh38
NC_000020.10:g.61982263_61982265del , CM000682.1:g.61982263_61982265del	GRCh37
NC_000020.9:g.61452707_61452709del	NCBI36
NG_011931.1:g.15435_15437del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.502_504del MANE Select	ENSP00000359285.4:p.Phe168del
ENST00000370263.8:c.502_504del	ENSP00000359285.4:p.Phe168del
ENST00000463705.5:n.1150_1152del
ENST00000467563.3:n.572_574del
ENST00000498043.6:c.526_528del
ENST00000615287.4:c.289_291del	ENSP00000483388.1:p.Phe97del
ENST00000627000.1:c.*191_*193del	ENSP00000486914.1:n.*191_*193del
ENST00000630240.1:n.223_225del
NM_000744.6:c.502_504del	NP_000735.1:p.Phe168del
NM_001256573.1:c.-27_-25del	NP_001243502.1:n.-27_-25del
NR_046317.1:n.758_760del
XM_011528524.1:c.289_291del	XP_011526826.1:p.Phe97del
XM_017027625.2:c.-27_-25del	XP_016883114.1:n.-27_-25del
XM_024451822.1:c.-27_-25del	XP_024307590.1:n.-27_-25del
NM_001256573.2:c.-27_-25del	NP_001243502.1:n.-27_-25del
NR_046317.2:n.711_713del
NM_000744.7:c.502_504del MANE Select	NP_000735.1:p.Phe168del