Canonical Allele Identifier: CA2189601882

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615706_78615709delinsAAAG , CM000677.2:g.78615706_78615709delinsAAAG	GRCh38
NC_000015.9:g.78908048_78908051delinsAAAG , CM000677.1:g.78908048_78908051delinsAAAG	GRCh37
NC_000015.8:g.76695103_76695106delinsAAAG	NCBI36
NG_016143.1:g.10587_10590delinsCTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1315_377+1318delinsCTTT MANE Select	ENSP00000315602.5:n.377+1315_377+1318deli...
ENST00000326828.5:c.377+1315_377+1318delinsCTTT	ENSP00000315602.5:n.377+1315_377+1318deli...
ENST00000348639.7:c.377+1315_377+1318delinsCTTT	ENSP00000267951.4:n.377+1315_377+1318deli...
ENST00000559658.5:c.377+1315_377+1318delinsCTTT	ENSP00000452896.1:n.377+1315_377+1318deli...
NM_000743.4:c.377+1315_377+1318delinsCTTT	NP_000734.2:n.377+1315_377+1318delinsCTTT...
NM_001166694.1:c.377+1315_377+1318delinsCTTT	NP_001160166.1:n.377+1315_377+1318delinsC...
NR_046313.1:n.878+1315_878+1318delinsCTTT
XM_006720382.1:c.176+1315_176+1318delinsCTTT	XP_006720445.1:n.176+1315_176+1318delinsC...
XM_011521173.1:c.296+1315_296+1318delinsCTTT	XP_011519475.1:n.296+1315_296+1318delinsC...
XM_006720382.3:c.176+1315_176+1318delinsCTTT	XP_006720445.1:n.176+1315_176+1318delinsC...
NM_000743.5:c.377+1315_377+1318delinsCTTT MANE Select	NP_000734.2:n.377+1315_377+1318delinsCTTT...
NM_001166694.2:c.377+1315_377+1318delinsCTTT	NP_001160166.1:n.377+1315_377+1318delinsC...
NR_046313.2:n.579+1315_579+1318delinsCTTT