Canonical Allele Identifier: CA2189601825

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78615598_78615600delinsACC , CM000677.2:g.78615598_78615600delinsACC	GRCh38
NC_000015.9:g.78907940_78907942delinsACC , CM000677.1:g.78907940_78907942delinsACC	GRCh37
NC_000015.8:g.76694995_76694997delinsACC	NCBI36
NG_016143.1:g.10696_10698delinsGGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.377+1424_377+1426delinsGGT MANE Select	ENSP00000315602.5:n.377+1424_377+1426deli...
ENST00000326828.5:c.377+1424_377+1426delinsGGT	ENSP00000315602.5:n.377+1424_377+1426deli...
ENST00000348639.7:c.377+1424_377+1426delinsGGT	ENSP00000267951.4:n.377+1424_377+1426deli...
ENST00000559658.5:c.377+1424_377+1426delinsGGT	ENSP00000452896.1:n.377+1424_377+1426deli...
NM_000743.4:c.377+1424_377+1426delinsGGT	NP_000734.2:n.377+1424_377+1426delinsGGT
NM_001166694.1:c.377+1424_377+1426delinsGGT	NP_001160166.1:n.377+1424_377+1426delinsG...
NR_046313.1:n.878+1424_878+1426delinsGGT
XM_006720382.1:c.176+1424_176+1426delinsGGT	XP_006720445.1:n.176+1424_176+1426delinsG...
XM_011521173.1:c.296+1424_296+1426delinsGGT	XP_011519475.1:n.296+1424_296+1426delinsG...
XM_006720382.3:c.176+1424_176+1426delinsGGT	XP_006720445.1:n.176+1424_176+1426delinsG...
NM_000743.5:c.377+1424_377+1426delinsGGT MANE Select	NP_000734.2:n.377+1424_377+1426delinsGGT
NM_001166694.2:c.377+1424_377+1426delinsGGT	NP_001160166.1:n.377+1424_377+1426delinsG...
NR_046313.2:n.579+1424_579+1426delinsGGT